Καριέρα

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Assurance to join our QA team in our offices in Limassol, Cyprus.

Καθήκοντα:

• Oversee and review change control processes and procedures, making recommendations for changes and/or improvements
• Review Batch records
• Assist in self-inspections and perform the follow up.
• Assist in external inspections
• Ensure that the monitoring environment is monitored and controlled by checking the following:
• The hygiene rules are followed by the personnel
  • Training programs are carried out
  • Gowning procedures are followed
  • All validations are carried out

Προσόντα:

University degree in a relevant scientific discipline such as Pharmacy, Chemistry, Biochemistry, Biology, etc. A postgraduate degree will be considered an advantage Experience in the field of pharmaceutical industry will be considered an advantage

Ability to clearly and concisely communicate technical information Ability to research, analyse and report independently across a breadth of topics Strong organisational skills and an eye for detail. Multi project handling at once under time pressure Good collaboration skills and team spirit Fluency in Greek and English language Strong IT Strong computer literacy skills

Benefits

A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Processes and Validation Technician to join our Quality Processes and Validation team in our offices in Limassol, Cyprus.

 

Καθήκοντα:

Prepare Process Validation Protocols and Reports Monitor the manufacturing process and prepare process observation reports Perform sampling Assist during process validation execution sampling by checking that sampling is performed according to the protocol and that the sampling forms are filled in correctly To label and gather all samples according to the protocols Assist in the preparation GAPs Analysis of the manufacturing process and equipment’s To compile and process data for Product Quality Review Report

 

Προσόντα:

A High School leaving Certificate or a diploma graduate Ability to clearly and concisely communicate technical information Ability to work in production environment  Strong organisational skills and an eye for detail. Multi project handling Ability to work under strict deadlines Good collaboration skills and team spirit Fluency in Greek and English language Strong IT Strong computer literacy skills Ιt would be considered a plus if you have:   Experience in the field of pharmaceutical

 

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Processes and Validation Associate to join our Quality Processes and Validation team in our offices in Limassol, Cyprus.

Καθήκοντα:

The Quality Process and Validation will have the opportunity to:   Prepare Process Validation Protocols and Reports Monitor the manufacturing process and prepare process observation reports Perform sampling Assist in the preparation of Risk Assessment of Elemental Impurities, Excipients Assist during process validation execution sampling by checking that sampling is performed according to the protocol and that the sampling forms are filled in correctly To label and gather all samples according to the protocols Assist in the preparation GAPs Analysis of the manufacturing process and equipment’s To compile and process data for Product Quality Review Report Assist in the preparation of the Product Quality Review Report Assist in the preparation of Continued (Ongoing) Process Verification Protocol and Reports

 

Προσόντα:

A University degree in a relevant scientific discipline such as Chemical Engineering, Pharmacy, Chemistry, Biochemistry, Biology Ability to clearly and concisely communicate technical information Ability to research, analyse and report independently across a range of topics Strong organisational skills and an eye for detail. Multi project handling Ability to work under strict deadlines Ability to work in production environment  Good collaboration skills and team spirit Fluency in Greek and English language Strong IT Strong computer literacy skills   Ιt would be considered a plus if you have: A postgraduate degree Experience in the field of pharmaceutical

 

If you believe that you have the above qualifications and this position sounds challenging, submit your application through the link below: http://www.medochemie.com/MainMenu/Careers.aspx   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We invite applications from highly motivated professionals for the position of R&D Associate/Specialist based in Limassol, Cyprus. 

Καθήκοντα:

• Overlook projects assigned, ensuring timely and effective execution
• Report on the progress of the projects as required
• Take part in cross-functional teams coordinating projects under responsibility

Προσόντα:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an advantage.
• Ability to work collaboratively in a team and prioritize work in a dynamic and fast-paced environment. 
• Very good interpersonal skills, analytical thinking and results orientation.
• Prior, relevant work experience will be a considered a plus but is not a pre-requisite. 
• Strong computer literacy
• Fluency in English (both verbal and written)

Benefits:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

  

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the most talented university students to join our summer internship scheme.  

What the Intern will get along the way:

• New skills, knowledge and work experience in a global pharmaceutical company
• Certificate of Completion upon successfully completing the internship

Καθήκοντα:

The Interns will work closely with a dedicated mentor who will guide them, assign meaningful tasks, and support their development throughout the programme.

The duties will vary according to the department the Intern will be placed.

The Company will accept applications for the summer internship programme for the below departments:
 
• Quality Control
• Research and Development
• Microbiology
• Regulatory Affairs
• Production
• Supply Chain

Προσόντα:

• Final or penultimate Year of an Undergraduate degree in Chemistry, Pharmacy, Biomedical, Biology, Chemical Engineering
• Excellent interpersonal and communication skills
• Excellent oral and written skills in English
• Excellent computer literacy (MS Office)

Applications will be accepted by 10/05/2025.

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.


We are seeking a dynamic and results-driven Medical Representative to promote Medochemie products to healthcare professionals, including doctors, pharmacists, and hospitals. The successful candidate will be responsible for building and maintaining strong relationships with clients, achieving sales targets, and providing scientific and technical information about our products.

Καθήκοντα:

• Promote the company's products portfolio within the entrusted territory to healthcare specialists, including doctors, pharmacists and hospitals.
• Maximize and achieve sales and performance indicator targets.
• Establish and maintain long-term strong relationships with healthcare specialists addressing any requirements or arising concerns.
• Participate in market intelligence activities and monitor/ analyze market trends, competitor activities, and customer feedback.
• Develops strong relationships with key decision makers and influencers.
• Organise CME sessions for healthcare specialists.
• Ensure compliance with industry regulations, company policies, and ethical standards.
• Provide timely reports on sales performance and market trends to management.

Προσόντα:

• Bachelor of Pharmacy from a recognized University
• Minimum 2 years of experience as a medical representative in Ethiopia.
• Experience in relevant therapeutic areas is advantageous (e.g. CVS, Anti-infective, Endocrine, CNS, and GI).
• Good achievement records, including customer engagement activities in the field.
• Excellent interpersonal and relationship-building abilities.
• Good territory planning and organising skills.
• Ability to work independently with minimum supervision and be a good Team player, result-oriented, proficient at planning and organizing, and capable of working independently.

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the most talented front desk assistant out there to join our team based in Limassol,Cyprus.

Καθήκοντα:

• Ensure and deliver high level of service to colleagues and associates
• Manage the call center
• Coordinate the appointments and communication with associates
• Management of correspondence/emails
• Oversee and supervise the reception area
• Assist the coordination of L&D programs, including scheduling and logistics, participants’ registration, and tracking participation and completion
• Assist subsidy programs run by the organization. (i.e. HRDA, Department of Labor, KEPA)
• Maintain L&D programs’ records in hardcopy and electronic format e.g.: certificates of attendance, attendance forms and training material
• Assist in the coordination of Wellbeing activities
• Provide additional office support if required

Προσόντα:

• Diploma in Secretarial Studies or other related fields
• Previous experience in a similar position
• Very good knowledge of Computers and MS Office
• Excellent knowledge of Greek and English language
• Customer-centric approach, consistency, courtesy and professional behavior

Benefits: Unique opportunities for career development in a fast-growing company Competitive remuneration package, including 13th salary, provident fund (employer’s contribution 7% of the monthly salary), bonding events and local celebrations Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ Modern and Professional Working Environment Optional participation in the Company’s Group Medical Scheme and Discount Scheme

 

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

Medochemie Ltd invites applications from career-oriented professionals for the position of Regulatory Affairs Specialist in our offices in Limassol.
 

Καθήκοντα:

• Responsible for the compilation of dossier sections and sourcing of relevant documentation for modules 2-5 of Medochemie dossiers intended for registration for Medochemie or clients at global scale in eCTD format
• Compilation of responses and scientific documentation at correspondences with authorities or clients related to initial submissions, and the lifecycle of submissions i.e. variations, renewals, upgrades and new developments. Monitoring the progress of responses related to Modules 2-5 deficiencies raised by the regulatory authorities
• Review of quality documentation related to Modules 2-5 for the applications in line with the appropriate guidelines and timelines
• CMC regulatory directions provision at the various company departments, external parties and suppliers for the projects which have been assigned
• Liaise with the appropriate departments within the company and external parties to collect all necessary information for the submission of pharmaceutical dossiers and product registration
• Assist in keeping the dossier core files (Modules 2-5 and corresponding QoS) fully up to date during registration procedures and variations
• Continuous follow up of the regulatory affairs activities of all projects that have been assigned. Update of the regulatory database in collaboration with the regulatory partners. • Understand and use the EU and International Regulatory guidelines
• Participate in the change control system and variation process according to the established internal workflow
• Participate in regulatory affairs internal projects of digital transformation, namely Regulatory Information management system and Submission Document Core Model
• Act as a member of responsible Regulatory team who is responsible for the submission of assigned regulatory projects
• Liaise with external Regulatory authorities and/or clients if required for the successful completion of projects
• Ensure policies and procedures are properly evaluated, implemented and carried out, safeguarding the compliance of company
• Support internal activities of Regulatory department in order to ensure regulatory compliance
• Monitoring the progress of the assigned projects and their finalization in a timely and accurate manner

Προσόντα:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• At least 2-3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs/CMC
• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment
• Strong communication, influencing and problem resolution skills.
• Strong organization skills and able to meet deadlines
• Ability to be adaptive to change, to multitask and give attention to detail
• Very good interpersonal skills, analytical thinking and result orientation
• Fluency in Greek and English (written and spoken) and computer literacy. Knowledge of any other languages will be considered an asset

Benefits:
 

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

 

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

Medochemie Ltd invites applications from career oriented professionals for the position of Regulatory Affairs Specialist in our offices in Athens, Greece.

Καθήκοντα:

• Responsible for the compilation of dossier sections and sourcing of relevant documentation for modules 2-5 of Medochemie dossiers intended for registration for Medochemie or clients at global scale in eCTD format
• Compilation of responses and scientific documentation at correspondences with authorities or clients related to initial submissions, and the lifecycle of submissions i.e. variations, renewals, upgrades and new developments. Monitoring the progress of responses related to Modules 2-5 deficiencies raised by the regulatory authorities
• Review of quality documentation related to Modules 2-5 for the applications in line with the appropriate guidelines and timelines
• CMC regulatory directions provision at the various company departments, external parties and suppliers for the projects which have been assigned
• Liaise with the appropriate departments within the company and external parties to collect all necessary information for the submission of pharmaceutical dossiers and product registration
• Assist in keeping the dossier core files (Modules 2-5 and corresponding QoS) fully up to date during registration procedures and variations
• Continuous follow up of the regulatory affairs activities of all projects that have been assigned. Update of the regulatory database in collaboration with the regulatory partners• Understand and use the EU and International Regulatory guidelines
• Participate in the change control system and variation process according to the established internal workflow
• Act as a member of responsible Regulatory team who is responsible for the submission of assigned regulatory projects
• Liaise with external Regulatory authorities and/or clients if required for the successful completion of projects
• Ensure policies and procedures are properly evaluated, implemented and carried out, safeguarding the compliance of company
• Support internal activities of Regulatory department in order to ensure regulatory compliance.
• Monitoring the progress of the assigned projects and their finalization in a timely and accurate manner

Προσόντα:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset
• At least 2-3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs/CMC
• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment
• Strong communication, influencing and problem resolution skills
• Strong organization skills and able to meet deadlines
• Ability to be adaptive to change, to multitask and give attention to detail
• Very good interpersonal skills, analytical thinking and result orientation
• Fluency in Greek and English (written and spoken) and computer literacy. Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

We are offering an attractive remuneration package (including medical insurance) and a challenging opportunity for professional development. Ability to become part of one of the most dynamic and prospective teams in the International Pharmaceutical industry in Cyprus / Greece.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees. We ‘re on a mission to find the best talent out there. We are now looking for a motivated and experienced QP to join our dynamic team in our offices in Limassol, Cyprus.

Καθήκοντα:

The Qualified Person will have the opportunity to: Certify that each batch of medicinal product complies with its marketing authorization, Good Manufacturing Practices (GMP), and other relevant legal requirements Ensure that testing, and manufacturing processes have been properly completed, and the relevant documentation has been reviewed before release for sale or use Ensure that any deviations or planned changes in production or quality control have been authorized by Quality Assurance, and their impact on the quality, safety and efficacy of the product and on the compliance with GMP and the marketing authorization, has been evaluated. Ensure that any changes requiring variation to the marketing or manufacturing authorization have been notified to and authorized by Regulatory Affairs as required Ensure that the manufacturing and testing processes have been validated Ensure that all necessary checks and tests have been performed, including any additional sampling, inspection, tests or checks initiated because of deviations or planned changes

 

Προσόντα:

Registered Qualified Person in Cyprus or another EU Member State Previous experience in the pharma industry as a qualified person Ability to interpret regulatory guidelines/legislation Highly organized; ability to multitask and process excellent time management skills Problem solving abilities Strong analytical and communication skills Proficient in the English language with excellent written and verbal communication skills Excellent computer literacy (MS Office)

 

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’   If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the best talent out there. We are now looking for a motivated Pharmacist to join our Quality Control team for our offices in Limassol,Cyprus.

Καθήκοντα:

The Pharmacist will have the opportunity to undertake the required training in view of becoming a Qualified Person. The training will last for 2 years and during these years you will have the opportunity to work in Quality Control and be trained on the full product lifecycle.

 
• To perform analysis on starting materials and bulk products of different dosage forms using a variety of analytical techniques including separation techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC)
• To carry out stability studies on finished products stored under different climatic control condition
• To be trained and familiarised with all GLP (Good Laboratory Practice), QC (Quality Control) and QA (Quality Assurance) GMP procedures
• To take part in the internal GMP trainings undertaken within the organization
• To take part in any training and required examination in view of becoming a Qualified Person in Medochemie Ltd

Upon obtaining your certificate, your duties will expand to the following: To certify that each batch of medicinal product complies with its marketing authorization, Good Manufacturing Practices (GMP), and other relevant legal requirements To ensure that testing, documentation, and manufacturing processes have been properly completed and reviewed before release for sale or use To ensure that any deviations or planned changes in any related GP (Good Practices) activities have been authorized by Quality Assurance To ensure that any changes requiring variation to the marketing or manufacturing authorization have been notified to and authorized by the relevant Regulatory agencies To ensure that the required validation and qualification activities have been performed satisfactorily

Προσόντα:

• Bachelor’s degree in Pharmacy
• Highly organized; ability to multitask and process excellent time management skills
• Problem solving abilities
• Strong analytical and communication skills
• Proficient in the English language with excellent written and verbal communication skills
• Excellent computer literacy (MS Office)

Benefits:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees. As part of our commitment to patient safety and regulatory compliance, we are looking for an experienced Pharmacovigilance Specialist to join our team and help us ensure the continued safety of our products.

 

Καθήκοντα:

 The Pharmacovigilance Specialist will have the opportunity to:
• Monitor and assess adverse drug reactions (ADRs) for the company's portfolio of generic medicines.
• Ensure timely and accurate submission of individual case safety reports (ICSRs) to Eudravigilance accordance with EU regulations.
• Collaborate with cross-functional teams (Quality Assurance, Regulatory Affairs, Medical affairs) to support safety data management and risk mitigation strategies.
• Maintain and update pharmacovigilance databases in compliance with Good Pharmacovigilance Practices (GVP).
• Prepare periodic safety update reports (PSURs), risk management plans (RMPs), and other safety documentation for regulatory submissions.
• Conduct signal detection and benefit-risk analysis for products on the market.
• Participate in pharmacovigilance audits and inspections, ensuring compliance with local and international regulatory requirements.
• Support the Pharmacovigilance Quality system by providing trainings, updating procedures, prepare and review contractual agreements as well as other quality related responsibilities, as per internal procedures.
• Support the QPPV with maintenance of the Pharmacovigilance System Master File.
• Stay up-to-date with changes in EU pharmacovigilance regulations and guidelines to ensure company-wide adherence.

Προσόντα:

• University degree in a Health-related field, including Pharmacy, life sciences or other related field.
• At least 2 years of experience within the pharmaceutical industry in pharmacovigilance, drug safety or regulatory affairs, preferably within the generic industry.
• Good knowledge of EU pharmacovigilance regulations, including GVP and ICH guidelines.
• Strong analytical skills with a focus on detail and accuracy.
• Excellent written and verbal communication skills in Greek and English.
• Ability to work independently and within a team, managing multiple projects under tight deadlines.
• Excellent computer literacy (MS Office)

Benefits:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

 If you wish to work in a pleasant, modern, professional environment with excellet career opportunities, please click Submit your CV or Fill in the Online Form.

 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for a motivated and skilled Laboratory Technician to join our Labs in our offices in Limassol, Cyprus.

Καθήκοντα:

The laboratory technician will have the opportunity to:
 
• Undertake administration work related to Labs
• Be responsible for Sample management (receipt and destruction)
• Undertake sampling of  Packing Materials
• Perform In-Process Control checks during packing
• Be trained and  follow  Laboratory Hygiene and Safety Guidelines

Προσόντα:

• High school certificate
• A certificate or bachelor’s degree would be considered as advantage
• Strong organization skills with a high attention to detail
• Proficient in the English and Greek language with excellent written and verbal communication skills
• Ability to work in Lab environment

Benefits:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you wish to work in a pleasant, modern, professional environment with excellet career opportunities, please click Submit your CV or Fill in the Online Form.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
 
All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for an Administrator to join our Quality Assurance team in our offices in Limassol, Cyprus.

Καθήκοντα:

The Administrator will have the opportunity to:
 
• Provide administrative support for tasks related to Quality Assurance
• Review batch documentation
• Carry out clerical work including typing, filing, copying and distribution of documents
• Ensure all procedures are carried out as per defined Standard Operating Procedures
• Undertake other tasks as required by the Quality Operations Senior Manager

Προσόντα:

• High School Certificate
•  Two/Three years Higher Education Certificate would be considered as a plus
• Ability to work in a closed environment as the office will be based inside the manufacturing site
• Strong attention to detail and problem-solving skills
• Highly organized; ability to multitask and process excellent time management skills
• Proficiency in the Greek and English language
• Excellent computer literacy (MS Office)

Benefits:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path'

 If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online form.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.   Είμαστε σε αποστολή να βρούμε ταλαντούχο Αποθηκάριο για να ενταχθεί στην ομάδα Εφοδιαστικής Αλυσίδας στα γραφεία μας στην Λεμεσό.

Καθήκοντα:

Ποια θα είναι τα καθήκοντα σου;   Υπεύθυνος /η για τον έλεγχο των αποθεμάτων πρώτων υλών και υλικών συσκευασίας, καθώς και ημιέτοιμου και έτοιμου προϊόντος στην αποθήκη. Βέλτιστη διαχείριση των πόρων που διαχειρίζεται. Διασφαλίζει τη σωστή διεξαγωγή των διαδικασιών όπως αυτές περιγράφονται στα Standard Operating Procedures (SOP’s) σύμφωνα με τους Κανόνες Καλής Παρασκευής (GMP). Μεριμνά για την ασφάλεια τόσο του προσωπικού όσο και των υλικών/προϊόντων της Εταιρείας. Βέλτιστη επικοινωνία με τα τμήματα παραγωγής και συσκευασίας για να διασφαλίζεται η συνεχής ροή προϊόντων. Ικανότητα να διαχειρίζεται πολλές παραγγελίες ή διαδικασίες ταυτόχρονα, χωρίς λάθη. Γρήγορη και αποτελεσματική αντιμετώπιση προβλημάτων. Δεξιότητες στη χρήση λογισμικών διαχείρισης αποθήκης και συστημάτων παρακολούθησης (π.χ. barcode scanners). Κατανόηση ηλεκτρονικών αρχείων και διαδικασιών εισαγωγής/εξαγωγής δεδομένων. Κατανόηση της χρήσης ειδικών συστημάτων για τη διαχείριση αποθεμάτων, όπως τα ERP συστήματα. Διασφαλίζει ότι το σύστημα ERP είναι πάντοτε σωστά ενημερωμένο και ανταποκρίνεται στη πραγματικότητα Διασφαλίζει αποτελεσματικές και αποδοτικές συνθήκες αποθήκευσης για όλα τα υλικά/προϊόντα στην αποθήκη.            Διασφαλίζει τη σωστή παρακολούθηση και έγκαιρη ενημέρωση στον ηλεκτρονικό υπολογιστή όλων των λογισμικών πράξεων που διεξάγονται στην αποθήκη. Εκδίδει έγκαιρα οποιαδήποτε έντυπα χρειάζονται από το Document Management System (DMS) Είναι υπεύθυνος και ενημερώνει τον Διευθυντή Αποθηκών για την κυκλική απογραφή αποθεμάτων Λαμβάνει μέρος στη Διαδικασία Καταγραφής των Αποθεμάτων. Συμπληρώνει έγκαιρα και έγκυρα όλα τα ημερολόγια καταγραφής (logbook) Λαμβάνει μέρος στη Διαδικασία Παραγγελιών υλικών/προϊόντων Εισηγείται σκέψεις/τρόπους για καλυτέρευση των διαδικασιών της Αποθήκης και της Εταιρείας γενικότερα. Αναλαμβάνει νέα ή αναπροσαρμοσμένα καθήκοντα σύμφωνα πάντα με τις ειδικές ανάγκες του Τμήματος Αποθηκών και της Εταιρείας γενικότερα. Εξασφαλίζει την ιχνηλασιμότητα των υλικών/προϊόντων και ακολουθεί το FEFO Εντοπίζει και αξιολογεί κίνδυνους που σχετίζονται με το χώρο που εποπτεύει

Προσόντα:

Απαραίτητα προσόντα για τη θέση:   Δίπλωμα σε Διοίκηση Εφοδιαστικής Αλυσίδας (Supply Chain Management), Διοίκηση Επιχειρήσεων, Οργάνωση, Διοίκηση Αποθηκών ή αλλον συναφή τομέα. Προηγούμενη τριετής εμπειρία σε Διαχείριση Λειτουργίας Αποθήκης. Πολύ καλή γνώση συστημάτων ERP και RF Scanner Πολύ καλή γνώση ηλεκτρονικών υπολογιστών και MS Office. Πολύ καλή γνώση της ελληνικής και αγγλικής γλώσσας. Πρωτοβουλία, ενδιαφέρον για προσωπική ανάπτυξη και διάθεση για συνεχή μάθηση. Ακεραιότητα χαρακτήρα, ομαδικό πνεύμα, υψηλό αίσθημα ευθύνης και προσοχή στη λεπτομέρεια.

Aν γίνεις μέλος της ομάδας μας θα έχεις τα πιο κάτω ωφελήματα:   Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία 13ος και 14ος μισθός Πληρωμένη Ετήσια Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον  Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.   Τμήμα:  Εφοδιαστικής Αλυσλιδας Τοποθεσία: Λεμεσός Κατάσταση Απασχόλησης: Πλήρης απασχόληση   Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Graphic Designer to join our Marketing team in our offices in Limassol.

Καθήκοντα:

The Graphic Designer will have the opportunity to:   Develop creative concepts and design solutions for various marketing materials and campaigns Create and optimize designs for digital and print media Collaborate with internal teams to align designs with brand guidelines and business objectives Stay up to date with design trends and industry best practices Manage multiple design projects and meet deadlines Maintain a consistent and high-quality design output across all platforms

 

Προσόντα:

Proven experience as a Graphic Designer Strong proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign, After Effects etc.) Solid understanding of typography, color theory, and layout principles Experience with web design and UI/UX principles is a plus Attention to detail and ability to work in a fast-paced environment Strong communication and collaboration skills A portfolio showcasing your design skills and experience

 

By joining us you can expect: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’   If you believe that you have the above qualifications and this position sounds challenging, submit your application through the link below: http://www.medochemie.com/MainMenu/Careers.aspx   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the best talent out there. We are now looking for a high qualified and motivated Learning and Development Senior Specialist to join our Human Resources team in our offices in Limassol,Cyprus.

Καθήκοντα:

• Assessing learning and development needs within the organization
• Drafting the L&D yearly plan and relevant budget
• Identifying subject matter experts and stakeholders to design and develop training programs
• Designing training curricula and training programs
• Organizing and delivering inductions,training sessions,workshops and seminars
• Monitoring and evaluating training and development programs' effectiveness
• Developing L&D strategy to serve long-term Company goals
• Developing policies and procedures on L&D topics
• Keeping up with the latest training and development trends and best practises
• Maintaining and ensure that is L&D management system up to date
• Utilizing any available subsidy schemes relevant to trainings or recruitment(i.e HRDA, Department of Labour, KEPA)
• Supporting L&D administration tasks concerning the full Learning and Development cycle
• Proposing ideas for events and other activities based on the Company's Wellbeing Strategy
• Writing and editing the in-house newsletters
• Acting as point of contact for employees and managers

Προσόντα:

• University degree in Human Resource Management, Psychology, Organizational Psychology, Occupational Psychology, Business Administration or any other related discipline
• HRDA Certified Trainer certificate (level 5) is required
• Minimum 5 years of experience in similar role
• Excellent presentation and facilitation abilities
• Good knowledge of HRDA subsidised schemes
• Maintains confidentiality and professional demeanour
• Strong computer literacy; proven experience in LMS platforms will be an advantage
• Fluency in both the Greek and English language

Benefits:
 

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you wish to work in a pleasant, modern, professional environment with excellet career opportunities, please click Submit your CV or Fill in the Online Form.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
 
All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Control Specialist to join our Quality Control team in our offices in Limassol, Cyprus.

Καθήκοντα:

Prepare SOPs and WINs for primary and secondary packaging materials Prepare specifications for primary and secondary packaging materials Review documentation related to packaging materials

 

Προσόντα:

University degree in Chemistry, Biochemistry, or another relevant field Ability to work under pressure Accountable and responsible Strong organization skills with a high attention to detail Εxcellent communication, interpersonal and teamworking skills High levels of ethics and integrity Proficient in the English and Greek language with excellent written and verbal communication skills Good working knowledge of the Microsoft Office tools

 

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path'  If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the form. Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Are you passionate about health and wellness?  Do you enjoy connecting with people? If so, we want you to be part of our dynamic team at Agetis Supplements, a food supplement company dedicated to enhancing lives through quality products.   AGETIS SUPPLEMENTS is a brand of nutritional supplements, established in Cyprus in 2005. With a portfolio of more than 40 products that cover a wide spectrum of needs in categories such as bones, muscles and joints, digestive health, immune system, skin care, heart and circulation, energy, sleep restoration and many more that ensure the consumers’ wellbeing, Agetis Supplements has presence in Europe, Asia, and Africa.  With innovative products of pharmaceutical-grade quality, Agetis products offer nutritional support using selected natural ingredients for optimal health.

Καθήκοντα:

Visit doctors and promote our innovative food supplement products. Build and maintain strong relationships with doctors, and clinics. Conduct product presentations and provide educational materials. Educate HCP’s on the role of food supplements s a trusted partner in supporting patients nutritional needs. Gather market insights and feedback to drive product development and marketing strategies. Collaborate with the sales team to achieve targets and expand market presence. Participate in company’s events.

 

Προσόντα:

Proven experience in medical sales or a related field. Strong communication and interpersonal skills with the ability to build and maintain relationships. A proactive attitude and a passion for health and nutrition. Ability to work independently and as part of a team. Very good knowledge of the English language and fluent in the Greek language. Excellent organization and time-management skills. Batchelor’s degree in Life Sciences, Pharmaceutical, Medicine or related field will be considered an advantage.

 

Benefits:

• A unique opportunity for a career in a fast-growing company 
• Competitive remuneration package based on qualifications and experience  
• 13th Salary 
• Paid Vacation 
• Modern & Professional Work Environment 
• Multiple events to bond with the team 
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary  
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme 
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ 

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted. 

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Production Shift Associate to join our Production Admin team in our offices in Limassol, Cyprus. 

Καθήκοντα:

• Coordinate, supervise and control production processes to ensure that products are produced according to the appropriate procedures in order to obtain the required quality 
• Monitor the compliance of the department with the requirements of Good Manufacturing Practice (GMP) 
• Carry out the production plan according to the production schedule 
• Supervise, coach, develop and monitor of the production personnel to ensure productivity and product quality 
• Follow and apply the requirements of the Good Manufacturing Practice (GMP)

 

Προσόντα:

• Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Pharmacy or other related field 
• Any previous experience in the pharmaceutical industry or in the specific field is desired; the position level will be defined based on experience
• Fluent in English language with excellent written and verbal communication skills 
• Excellent analytical and technical skills related to this discipline 
• Excellent problem-solving and analytical skills 
• Ability to work under pressure Accountable and responsible 
• An enthusiastic team player with a strong drive to create a positive and collaborative work environment 

 

Benefits: 

• A unique opportunity for a career in a fast-growing company 
• Competitive remuneration package based on qualifications and experience  
• 13th Salary 
• Paid Vacation 
• Modern & Professional Work Environment 
• Multiple events to bond with the team 
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary  
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme 
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ 

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted. 

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.

Καθήκοντα:

Φύτεμα, πότισμα και περιποίηση φυτών Κλάδεμα δέντρων και θάμνων κούρεμα και πότισμα γκαζόν Χρήση Γεωργικών εργαλείων και λιπασμάτων Καθαρισμός ξερών λουλουδιών και φύλλων Λίπανση και ψεκασμός για όλα τα είδη των φυτών

 
 

Προσόντα:

Απολυτήριο λυκείου ή Τεχνικής σχολής Κάτοχος άδειας οδήγησης Γνώσεις σε χρήση μηχανημάτων κηπουρικής Προηγούμενη εμπειρία τουλάχιστο 3 χρόνια  σε ίδια/παρόμοια θέση Υπευθυνότητα και εργατικότητα Ευχάριστος, επικοινωνιακός χαρακτήρας   Καλή γνώση Αγγλικής & Ελληνικής γλώσσας επικοινωνίας Θα θεωρηθεί πλεονέκτημα εάν έχεις:   Πτυχίο Γεωπονίας

 

Ωφελήματα:    Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία 13ος μισθός Ετήσια Πληρωμένη Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας   Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.   Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.

Η φαρμακευτική εταιρεία MEDOCHEMIE HELLAS A.E. είναι θυγατρική εταιρεία της MEDOCHEMIE Ltd, η οποία εργοδοτεί 2000 επαγγελματίες, διατηρεί γραφεία σε 19 χώρες και εξάγει τα προϊόντα της σε 122 χώρες.  Διαθέτει 5145 άδειες κυκλοφορίας και 500 διαφορετικούς συνδυασμούς προϊόντων, οι οποίοι ταξινομούνται σε 10 θεραπευτικές κατηγορίες που περιλαμβάνουν συνταγογραφούμενα και μη συνταγογραφούμενα φάρμακα (OTC).  

Η φαρμακοβιομηχανία Medochemie Ltd διαθέτει 15 παραγωγικές μονάδες, με πιστοποίηση EU GMP – WHO (European Good Manufacturing Practices – World Health Organization), 9 στην Κύπρο, 1 στην Ολλανδία και 5 στο Βιετνάμ, και καταγράφει κορυφαίες επιδόσεις στην παραγωγή, εμπορία, διανομή και εξαγωγή επώνυμων αδειοδοτημένων ομοιοδραστικών φαρμάκων.

H MEDOCHEMIE HELLAS A.E. ζητά να προσλάβει άμεσα Επιστημονικό Συνεργάτη με έδρα την Αθήνα.

 
 

Καθήκοντα:

Η επίτευξη του πλάνου πωλήσεων της εταιρείας στις περιοχές ευθύνης του, μέσω της αποτελεσματικής υλοποίησης της ισχύουσας στρατηγικής και της εφαρμογής των εκάστοτε πολιτικών

Προσόντα:

• Εμπειρία μεγαλύτερη των 2 ετών σε πωλήσεις
• Προηγούμενη εμπειρία στις πωλήσεις φαρμακευτικών προϊόντων και εμπειρία στον διαβήτη, θα θεωρηθεί επιπλέον προσόν
• Επιθυμητό πτυχίο ΑΕΙ
• Ικανότητα επικοινωνίας και ανάπτυξης διαπροσωπικών σχέσεων, αναλυτική σκέψη και φιλοσοφία προσανατολισμένη στο αποτέλεσμα
• Επαγγελματική συνέπεια και ικανότητα εργασίας υπό πίεση
• Εξαιρετική γνώση Η/Υ

 Ωφελήματα:
 

• Ανταγωνιστικό πακέτο αποδοχών και κινήτρων (bonus)
• Εταιρικό αυτοκίνητο
• Κινητό τηλέφωνο
• Πρόσθετη ιατροφαρμακευτική κάλυψη
• Δυνατότητα συνεχιζόμενης εκπαίδευσης
• Προοπτικές εξέλιξης

 Οι ενδιαφερόμενοι/ες μπορούν να αποστείλουν το βιογραφικό τους σημείωμα στο σύνδεσμο  ΥΠΟΒΟΛΗ ΒΙΟΓΡΑΦΙΚΟΥ ΣΗΜΕΙΩΜΑΤΟΣ .
 
Οι υποψήφιοι να σημειώσουν ότι βασιζόμενοι στον Γενικό Κανονισμό Προστασίας Προσωπικών Δεδομένων (GDPR), όλες οι αιτήσεις/βιογραφικά που είχαν καταχωρηθεί στη βάση μας, έχουν διαγραφεί. Στην περίπτωση που είχατε αποστείλει παλαιότερα το βιογραφικό σας και σας ενδιαφέρει η συγκεκριμένη θέση, παρακαλώ συμπληρώστε ξανά την αίτηση.

Όλες οι αιτήσεις θα εξεταστούν και θα θεωρηθούν αυστηρά εμπιστευτικές.
 

Medochemie Romania SRL is looking for a professional and motivated colleague to join our team for the position of Product Manager Diabetes/CNS. Reporting to the Business Retail BUM, the Product Manager will develop and implement long-term and short-term marketing plans, aimed at maximizing both the specific objectives of the products in the portfolio, as well as increasing their market share.

We ‘re on a mission to find the best talent out there. We are now looking for an experienced Product Manager to join our Sales team in our offices in Romania.

Καθήκοντα:

• Proactive development of the marketing and promotion mix to meet all agreed brand objectives and customer needs.
• Regular performance monitoring through appropriate tools and implementation of corrective actions, if necessary.
• Creation and delivery of operational plans appropriate to the life cycle of the products to optimize the profitability of the company.
• Advanced understanding and use of all major marketing principles and processes in terms of portfolio management.
• Development of the clients' perspective through appropriate techniques and/or tools.
• Provides Medical Representatives with the necessary support to achieve their goals.
• Creates and develops project calendars for assigned products and all new releases.
• Organizes the training courses for the products in the portfolio.

Προσόντα:

• Strong experience and excellent professional results in pharmaceutical marketing (Diabetes / CNS are the preferred therapeutic areas);
• Adequate higher studies in the medical field/Marketing;
• Very strong communication skills and leadership potential;
• Excellent negotiation, presentation and relationship building skills;
• Orientation towards the client and result;
• Oriented towards working in a team;
• Advanced level of knowledge of the English language;
• Good computer skills (master in Excel and Power Point).

Benefits: • The opportunity to work in a prestigious international pharmaceutical company. • Opportunities for professional development and career growth. • Competitive remuneration based on results; • Health and life insurance Based on the General Data Protection Regulation (GDPR), the personal information we collect from candidates is used for the purpose of processing in connection with the recruitment process of Medochemie Romania SRL. This information is kept safe with an appropriate level of security and for as long as we need it for legitimate commercial and legal reasons. Then we will delete them safely and securely.

By applying for this vacancy, you agree that Medochemie Romania SRL will process your personal data in connection with this application.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Research and Development Associate to join our Research and Development team  either in our offices in Limassol or Athens.

Καθήκοντα:

Critical review of documentation provided by active substance suppliers (incl. synthetic route), providing comments on compliance with current regulations and guidelines Evaluation of the risk for Nitrosamine impurities based on the structure of a molecule and the conditions existing in the synthetic route of the active substance or the manufacturing process of the finished product Contribution in cross-functional projects, by providing feedback on the possible degradation pathways of a molecule and the possible impurities that could be formed in the active substance or the finished product Support with expert opinion on the most appropriate specifications for impurities in the active substance as well as the finished product, for new product developments

 

Προσόντα:

University degree in Chemistry, Pharmacy or other relevant science degree with a strong focus on organic chemistry. A postgraduate degree will be considered as an advantage. Prior, relevant work experience will be a considered a plus, but is not a pre-requisite. Ability to work collaboratively in a team and prioritize work in a dynamic and fast-paced environment. Very good interpersonal skills, analytical thinking and results orientation. Strong computer literacy Fluency in Greek & English

 

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’   If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.
 
Είμαστε σε αποστολή να βρούμε Φύλακα/Θυρωρό για να ενταχθεί στην ομάδα μας στα γραφεία μας στην Λεμεσό, Κύπρο.

Καθήκοντα:

• Επιτήρηση και έλεγχος εγκαταστάσεων Εταιρείας
• Έλεγχος πρόσβασης ατόμων και οχημάτων
• Διαχείριση συστήματος πυρανίχνευσης

Προσόντα:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης
• Απαραίτητη Άδεια άσκησης του επαγγέλματος Ιδιώτη Φύλακα
• Τουλάχιστον 2 χρόνια προϋπηρεσία
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα
• Δυνατότητα εργασίας σε βάρδια Πρωινό / Απογευματινό / Νυχτερινό : Δευτέρα- Κυριακή: 07:00-15:00/ 15:00-23:00/ 23:00-07:00

Ωφελήματα

Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία 13ος και 14ος Μισθός Πληρωμένη Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Προαιρετική Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.   Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.     Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

 

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   Η Medochemie Ltd ζητά να προσλάβει υπεύθυνα και συνεργάσιμα άτομα με έδρα την Λεμεσό, για τη θέση Production Assistant:

Καθήκοντα:

• Υποστήριξη της διευθυντικής ομάδας παραγωγής
• Ετοιμασία των εγγράφων που απαιτούνται για τη διαδικασία παραγωγής.
• Καταχώρηση δεδομένων σε ηλεκτρονικά αρχεία που αφορούν την παραγωγή.
• Έλεγχος αποθεμάτων.
• Χρήση ηλεκτρονικού συστήματος
• Αρχειοθέτηση εγγράφων παραγωγής και φακέλων προσωπικού

Προσόντα:

Πολύ καλή γνώση Ελληνικής και Αγγλικής γλώσσας. Πολύ καλές γνώσεις Ηλεκτρονικών Υπολογιστών. Ικανότητα διαχείρισης πολλών πραγμάτων ταυτόχρονα. Παρατηρητικότητα και ομαδικότητα Θα θεωρηθεί πλεονέκτημα εάν έχεις:  Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση

 Ωφελήματα:
 

• Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία
• Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας
• Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία
• 13ος
• Πληρωμένη Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

 

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση. Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτή η θέση ακούγεται πρόκληση, υποβάλετε την αίτησή σας μέσω του παρακάτω συνδέσμου: (for portals) http://www.medochemie.com/MainMenu/Careers.aspx   Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.   Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees. We ‘re on a mission to find the best talent out there. We are now looking for a talented Graphic Designer to join our Marketing team in our offices in Limassol, Cyprus.

Καθήκοντα:

Design and implementation of the packaging design in accordance with the corporate identity (cartons, leaflets, aluminium foils, labels, tubes), from concept through to production Follow corporate branding procedures and country specific regulations for pharmaceutical products Time-manage multiple projects and keep stakeholders updated on progress Work independently as well as cooperatively with internal and external stakeholders to meet deadlines and schedule project implementation based on workload Update and maintain internal databases as per department procedures

 

Προσόντα:

Bachelor’s degree (or equivalent) in graphic design, art, or related discipline. A post graduate degree will be considered an advantage. Minimum 2 years of experience in graphic design. Experience in the pharmaceutical sector will be considered an advantage. Expertise with graphic design software such as Corel Draw or Adobe Creative Cloud (Illustrator, Photoshop) Ability to clearly and concisely communicate technical information Organizational and time-management skills for meeting deadlines in a fast-paced environment as well the ability to handle multiple projects Very good knowledge of the English language, both in written and verbal Desire to continue building skill set with education and training Have a strong drive to create a positive and collaborative work environment

 

Benefits:

A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations, and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
 
We ‘re on a mission to find the best talent out there. We are now looking for a talented Research and Development Associate to join our Research and Development team in our offices in Limassol, Cyprus.

Καθήκοντα:

To conduct research, develop and optimize analytical methods for the characterization of APIs and related compounds using a variety of analytical and separation techniques such as High Performance Liquid Chromatography (HPLC), LC-MS/MS and Gas Chromatography (GC). Perform physical and chemical analysis for analytical and product development and follow all the guidelines on Good Laboratory Practice (GLP) Conduct a preliminary and limited quality evaluation of the raw material and Finished product tested for R&D purposes in accordance with the current guidelines in force. Apply basic regulatory knowledge under which the medical products are governed. Prepare analytical plan and protocol. Compile consolidated summaries and provide required reports throughout the development of each product. Perform detailed literature searches and review all available literature data for the development of analytical and product development.

 

Προσόντα:

University degree in Pharmaceutical Chemistry or Chemistry or other relevant field. PhD or Master in analytical chemistry will be considered as an additional asset. Very good R&D thinking and result orientation Accountable and Responsible Ability to work under pressure Excellent communication, interpersonal and teamworking skills High levels of ethics and integrity Proficient in the English and Greek language with excellent written and verbal communication skills Good working knowledge of the Microsoft Office tools

 

Benefits:   A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’  If you believe that you have the above qualifications and this opening sound challening apply now by uploading your CV below or by completing the online application. Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 13 ultramodern manufacturing plants, 9 in Cyprus, 3 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities. We ‘re on a mission to find the best talent out there. We are now looking for a talented Supply Chain Specialist to join our Supply Chain team in our offices in Limassol, Cyprus.

Καθήκοντα:

The Supply Chain Specialist will have the opportunity to:   Coordinate the production workflow for one or multiple products Create and maintain a constrained production schedule and ensure raw material availability Create efficient scheduling processes or methods to attain production goals Handle all production issues in a way that it doesn’t hinder production and delivery Identify issues or areas of improvement and suggest alternative ways to improve the existing processes Collect and analyse data and use software to generate production reports Ensure that company deadlines are met

 

Προσόντα:

Bachelor’s degree in Chemical Engineering, Mathematics, or any other related field Ability to handle and prioritize multiple tasks Excellent organisational and numeracy skills Strong knowledge of Excel and any other Microsoft Office tools Strong computer literacy Fluency in Greek and English language It would be considered a plus if you have:   Previous experience in the supply chain in the pharmaceutical sector Knowledge of MS Project

 

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.    All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.   Είμαστε σε αποστολή να βρούμε ταλαντούχο Χειριστή Μηχανών για να ενταχθεί στην ομάδα Παραγωγής μας στα γραφεία μας στην Λεμεσό, Κύπρο.

Καθήκοντα:

Ρύθμιση, επίβλεψη λειτουργίας και καθαρισμός μηχανών παραγωγής φαρμακευτικών σκευασμάτων Τήρηση των Κανόνων Καλής Παρασκευής Φαρμάκων (GMP) κατά τη διαδικασία παραγωγής Καταχώρηση δεδομένων στις εντολές παρτίδας παραγωγής, στα απαιτούμενα έντυπα και ημερολόγια

 

Προσόντα:

Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών Ευχάριστος, επικοινωνιακός χαρακτήρας που να μπορεί να λειτουργεί ομαδικά αλλά και ατομικά Προσοχή στην λεπτομέρεια Υπευθυνότητα και εργατικότητα

 
• Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν

Δυνατότητα εργασίας σε βάρδιες είναι απαραίτητη (ωράρια  Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)

 

Ωφελήματα:   Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία 13ος και 14ος Μισθός Πληρωμένη Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Προαιρετική Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.   Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.     Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

Medochemie Hellas is looking for a talented and career-oriented Medical Sales Representative for the area of Athens, Greece
 

Καθήκοντα:

• Achieve company’s sales plan in assigned area by implementing existing strategy and policies

Προσόντα:

• At least 3 years of experience in sales
• Prior experience in similar position and experience in diabetes products will be considered an asset
• University degree would be appreciated
• Very good interpersonal and influence skills, analytical thinking and results orientation
• Business acumen and ability to work under pressure
• PC Literacy

Benefits:

• Competitive remuneration package and bonus
• Company car
• Company mobile
• Group private medical scheme
• Ongoing training
• Career growth opportunities

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.

 

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated with strict confidentiality

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

 

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.
 
We ‘re on a mission to find the best talent out there. We are now looking for a talented Packing Shift Associate to join our Packing Admin team in our offices in Limassol, Cyprus.

Καθήκοντα:

Coordinate, supervise and control packing processes to ensure that products are packed according to the appropriate procedures in order to obtain the required quality. Monitor and apply  the compliance of the department with the requirements of Good Manufacturing Practice (GMP) Carry out the packing plan according to the packing schedule. Supervise, coach, develop and monitor of the packing personnel to ensure productivity and product quality.


 

Προσόντα:

• Bachelor’s degree in Mechanical Engineering ,  Chemical engineering, Industrial Pharmacy, Pharmacy or other related field
• Any previous experience in the pharmaceutical industry or in the specific field is desired; the position level will be defined based on experience
• Excellent analytical and technical skills related to this discipline
• Ability to work under pressure
• Accountable and responsible
• An enthusiastic team player with a strong drive to create a positive and collaborative work environment
• Proficient in the English language with excellent written and verbal communication skills
 

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ 

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application. 

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.
 

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 5145 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 122 χώρες σε όλο τον κόσμο. Οι δεκαπέντε ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.
 

Είμαστε σε αποστολή να βρούμε Προσωπικό Συσκευασίας για να ενταχθεί στο τμήμα Συσκευασίας στα εργοστάσια μας στην Λεμεσό, σε πρωινή ή/και απογευματινή βάρδια (ωράρια  Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00 (εκ περιτροπής ανά εβδομάδα).

Καθήκοντα:

 

Συναρμολόγηση, συσκευασία και αποθήκευση φαρμακευτικών σκευασμάτων Χειρισμός μηχανημάτων συναρμολόγησης και συσκευασίας Καταχώρηση δεδομένων στις εντολές παρτίδας παραγωγής, στα απαιτούμενα έντυπα και ημερολόγια

 

Προσόντα:

Καλή γνώση της ελληνικής γλώσσας (προφορική και γραπτή) Βασικές γνώσεις της Αγγλικής γλώσσας Ευχάριστος, επικοινωνιακός χαρακτήρας που να μπορεί να λειτουργεί ομαδικά Προσοχή στην λεπτομέρεια Θα θεωρηθεί πλεονέκτημα εάν έχεις:   Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση.

 
 

Ωφελήματα

Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας 13ος και 14ος Μισθός Επίδομα απογευματινής βάρδιας 15% Πληρωμένη Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.

 Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.

Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Κατόπιν αξιολόγησης, θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.   Είμαστε σε αποστολή να βρούμε ταλαντούχο Engineering Associate για να ενταχθεί στην ομάδα μας στην Λεμεσό, Κύπρο.

Καθήκοντα:

Εκπόνηση και υλοποίηση προγραμμάτων προληπτικής συντήρησης Υπεύθυνος για την συντήρηση των μηχανήματων παραγωγής , συσκευασίας και βοηθητικών εγκαταστάσεων  Επίλυση προβλημάτων που προκύπτουν κατά τη λειτουργία των μηχανών (βλάβες, ρυθμίσεις κλπ) Δημιουργία και εφαρμογή διαδικασιών λειτουργίας και συντήρησης εξοπλισμού

 

Προσόντα:

Κάτοχος πτυχίου Μηχανολόγου Μηχανικού, Ηλεκτρολόγου Μηχανικού, Ηλεκτρονικού Μηχανικού Προηγούμενη πείρα στην φαρμακοβιομηχανία θα θεωρηθεί επιπρόσθετο προσόν Καλή γνώση της Αγγλική γλώσσας Καλή γνώση Ηλεκτρονικών Υπολογιστών Ικανότητα πολλαπλών εργασιών, ικανότητα διαχείρισης χρόνου αποτελεσματικά Ικανότητα να δουλεύει υπό πίεση Ευχάριστος, επικοινωνιακός χαρακτήρας που να μπορεί να λειτουργεί ομαδικά αλλά και ατομικά Δυνατότητα εργασίας σε βάρδιες

 

Ωφελήματα:

Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία 13ος Μισθός Πληρωμένη Άδεια Πολλαπλές Δραστηριότητες με την ομάδα Προαιρετική Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον     Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.     Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.     Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Junior IT Technician to join our IT team in our offices in Limassol,Cyprus .

Καθήκοντα:

Install, configure, and maintain software and hardware components Install, configure, and support copiers, fax machines, printers, scanners and miscellaneous peripheral hardware Provide 1st level support to users for all computer hardware and software issues or queries Troubleshoot software and hardware systems, such as computers/laptops, telephony systems and network devices Repair and or replace damaged computer and/or network components Maintain the up-to-date technical documentation Desktop OS administration/ network operating systems Carries out any further duties assigned

 

Προσόντα:

Relevant certificates or College Diploma in Computer Engineering/Computer Science Previous experience in a relevant role will be considered as an advantage Experience with Active directory, Exchange and Windows Infrastructure, Cisco Technologies will be considered as an advantage Very good interpersonal skills and customer-oriented attitude Fluency in both written and spoken English and Greek

 

Τοποθεσία: Limassol,Cyprus

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’   If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

 

Καθήκοντα:

• Search in available patent databases in order to check the status of patent applications, litigations etc in both European and non - European territories
• Review, analyze and inform on patent restrictions and prepare consolidated patent reports with due diligence 
• Search for the patent regulations in force in each country for new or existing products   
• Assess and conclude on active pharmaceutical substances patents pertinent to their synthetic schemes and physical properties, on finished dosage forms compositions, indications, manufacturing processes  etc towards any valid patents
• Prepare high quality and substantiated advices on the new products strategies in terms of patent restrictions and specific issues that need to be taken into consideration

Προσόντα:

• University degree in Chemistry, Pharmacy or a related field. A postgraduate degree will be considered an advantage
• Minimum of 5 years’ experience as patent specialist in generic medicines is a must. Experience in European Intellectual Property environment will be considered as an additional asset.
• Ability to work collaboratively in a team 
• Ability to multitask and work under pressure
• Excellent interpersonal and communication skills
•  Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.   All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Microbiologist to join our Microbiology  team in our offices in Limassol .

Καθήκοντα:

The Microbiologist will have the opportunity to:

 
• Perform Microbiological testing on Pharmaceutical  products and document all records.
• Develop and prepare Validation protocols for new test methods.
• Perform test on water samples, bulk products and starting materials and document all records.
• Maintain accurate records and perform all tests under GMP guidelines
• Maintain  purchase orders for consumables used and monitor inventory
• Continuous familiarization with Pharmacopeia and Guideline papers to ensure adherence to current procedures

Προσόντα:

University degree in Microbiology. A postgraduate degree will be considered as an advantage At least one year of experience in pharmaceutical microbiological testing or food industry microbiological testing Excellent command of the Greek and English language, both written and oral Excellent communication and interpersonal skills Ability to work collaboratively in a team and prioritize work in a dynamic and fast-moving environment. Ability to work under pressure and meet deadlines Exceptional attention to detail

 

Τοποθεσία: Limassol,Cyprus

Benefits:

A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 13 ultramodern manufacturing plants, 9 in Cyprus, 3 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Pharmaceutical Representative to join our Sales team to cover Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.

 

Καθήκοντα:

• Conducts visits to pharmacies for the proper promotion of the medical products
• Maintains existing business and presents new products
• Develops and maintain positive clients relationships
• Organizes and participates in medical events
• Solves any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

Προσόντα:

• Licensed Medical Representatives with at least two years of experience in a similar position.
• University degree in Pharmacy, Biology, Chemistry, Medical Representative or other relevant disciplines will be considered as an additional asset.
• Excellent level of knowledge of the Greek and the English language.
• Very good interpersonal and influence skills, analytical thinking, results orientation.

Καθήκοντα:

• Conducts visits to doctors for the proper promotion of the medical products
• Maintains existing business and presents new products
• Develops and maintain positive clients relationships
• Organizes and participates in medical events
• Solves any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

Προσόντα:

• Licensed Medical Representatives with at least two years of experience in a similar position.
• University degree in Pharmacy, Biology, Chemistry, Medical Representative or other relevant disciplines will be considered as an additional asset.
• Excellent level of knowledge of the Greek and the English language.
• Very good interpersonal and influence skills, analytical thinking, results orientation.

A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th Salary Paid Vacation Modern & Professional Work Environment Multiple events to bond with the team Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary Optional participation in the Company’s Group Medical Scheme, and Discount Scheme Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’  If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.   Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.     All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.
 
Η Medochemie Ltd ζητά να προσλάβει υπεύθυνα και συνεργάσιμα άτομα με έδρα την Λεμεσό, για τη θέση Προσωπικό τμήματος Καθαριότητας:
 

Καθήκοντα:

• Καθαρισμός γραφείων, τουαλετών, κουζίνας, διαδρόμων και σκάλων
• Καθαρισμός χώρων αποθήκης (αποδυτηρίων, γραφείων και διαδρόμων) βάσει του προτύπου SOP
• Καθαρισμός χώρων παραγωγής (αποδυτηρίων, γραφείων, διαδρόμων και Μηχανοστασίων) βάσει του προτύπου SOP
• Φροντίδα και συντήρηση των εργοστασιακών στολών
• Καθαριότητα εξωτερικών χώρων

Προσόντα:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης
• Βασικές γνώσεις της Αγγλικής γλώσσας
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Ωφελήματα:
 

• Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία
• Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας
• Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία
• 13ος Μισθός
• Πληρωμένη Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης 
•  Συμμετοχή στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.

 Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.

Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Κατόπιν αξιολόγησης, θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.   We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Control Associate to join our Quality Control team in our offices in Limassol, Cyprus.

Καθήκοντα:

To perform chemical analysis to raw materials and finished pharmaceutical dosage forms using a variety of analytical and separation techniques such as High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). To carry out stability studies to pharmaceutical products stored under different climatic control conditions following the appropriate monitoring software, using the required analytical & separation technique and implementing analytical chemistry statistics. Use of statistical tools to monitor trends will be considered as an asset To follow all the guideline’s on Good Laboratory Practice (GLP)

 

Προσόντα:

University degree in Chemistry, Biochemistry or other relevant field. Post Graduate diploma will be considered as asset. Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, will be considered as an additional asset. Effective verbal and written communication skills Fluency in  Greek and English language Computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation.

 

Benefits
 

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.