Careers

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 3800 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 Pharmaceutical Intellectual Property Manager to join our team in our offices in Athens,Greece.
 

Duties:

The Pharmaceutical Intellectual Property Manager will have the opportunity to:
 
• 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

Qualifications:

• 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 an advantage
• 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

Location: Athens,Greece

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 headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 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 Pharmaceutical Intellectual Property Manager to join our team in our offices in Amman, Jordan.

Duties:

The Pharmaceutical Intellectual Property Manager will have the opportunity to:
 
• 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

Qualifications:

• 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 an advantage
• 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

Location: Amman, Jordan

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 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).

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

Duties:

• Be responsible for the CMC compilation of dossiers and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force.
• Have a key role representing under supervision Regulatory Affairs in the Interdepartmental Team whose aim is to successfully transfer the manufacturing processes and analytical methods between different Medochemie Manufacturing Sites
• Successfully maintain dossiers’s lifecycle.

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• At least 3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs or QA.
• 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
• 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

Location: Athens, Greece

We are offering an attractive remuneration package (including medical insurance) and a challenging opportunity for professional development.
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 wtih 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 3800 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 Clinical Manager (Bio Equivalence Expert) to join our team in any of our offices in Bucharest, Athens, Limassol, Sofia, Amman, Cairo.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

• University degree in Medicine, Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
It would be considered a plus if you have:
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset.
 
 

Location: SOFIA, BULGARIA

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 
• Modern & Professional Work Environment 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 Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 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 Clinical Manager (Bio Equivalence Expert) to join our team in any of our offices in Bucharest, Athens, Limassol, Sofia, Amman, Cairo.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

What does it take to do the job?
 
• University degree in Medicine , Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
 
It would be considered a plus if you have:
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset.

Location: Amman, Jordan

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 
• Modern & Professional Work Environment 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 Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 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 Clinical Manager (Bio Equivalence Expert) to join our team in any of our offices in Bucharest, Athens, Limassol, Sofia, Amman, Cairo.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

• University degree in Medicine , Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
It would be considered an advantage if you have:
 
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset

Location: Cairo, Egypt

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 
• Modern & Professional Work Environment 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 Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 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 Clinical Manager (Bio Equivalence Expert) to join our team in any of our offices in Bucharest, Athens, Limassol, Sofia, Amman, Cairo.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

• University degree in Medicine , Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
It would be considered a plus if you have:
 
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset

Location: Athens, Greece

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 
• Modern & Professional Work Environment 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 Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 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 Clinical Manager (Bio Equivalence Expert) to join our team in any of our offices in Bucharest, Athens, Limassol, Sofia, Amman, Cairo.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

• University degree in Medicine , Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
It would be considered a plus if you have:
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset.


 

Location: Bucharest, Romania

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 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).

Medochemie Hellas, affiliate company of Medochemie Ltd, is looking for a talented and career-oriented Medical Sales Representative for the area of Korinthos, Greece

Duties:

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

Qualifications:

•  University degree would be considered an advantage
• At least 3 years of experience in sales
• Prior experience in similar position and experience in diabetes products will be considered an advantage
• Very good interpersonal and influence skills, analytical thinking and results orientation
• Business acumen and ability to work under pressure
• Excellent interpersonal and communication skills
• Excellent computer literacy (MSOffice)

Location: Korinthos, Greece

Benefits:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• Modern & Professional Work Environment
• Optional participation in the Company’s Group Medical Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’
• Company car
• Company mobile

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 (GDPR), all applications/CVs are kept in our databse 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).

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

Duties:

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

Qualifications:

•  University degree would be considered an advantage
• At least 3 years of experience in sales
• Prior experience in similar position and experience in diabetes products will be considered an advantage
• Very good interpersonal and influence skills, analytical thinking and results orientation
• Business acumen and ability to work under pressure
• Excellent interpersonal and communication skills
• Excellent computer literacy (MSOffice)

Location: Athens, Greece

Benefits:
 

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• Modern & Professional Work Environment
• Optional participation in the Company’s Group Medical Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’
• Company car
• Company mobile

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 (GDPR), all applications/CVs are kept in our databse 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 3800 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 invite applications from highly qualified and motivated professionals for the position of  Patent Specialist based in Cairo, Egypt.  
 

Duties:

• 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

Qualifications:

• 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

Location: CAIRO,EGYPT

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 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 φαρμακευτική εταιρεία MEDOCHEMIE HELLAS A.E. είναι θυγατρική εταιρεία της MEDOCHEMIE Ltd, που εξειδικεύεται στην παραγωγή/εμπορία γενοσήμων φαρμάκων και συμπληρωμάτων διατροφής. Η εταιρεία δραστηριοποιείται σε πάνω από 107 χώρες, έχοντας 13 δικές της μονάδες παραγωγής στην Κύπρο,την Ολλανδία και την Ασία. Διαθέτει στο χαρτοφυλάκιό της 630 εγκεκριμένα προϊόντα και πάνω από 4.355 εγγραφές προϊόντων παγκοσμίως.   H MEDOCHEMIE HELLAS A.E. στοχεύοντας στην περαιτέρω ανάπτυξή της ζητά να προσλάβει άμεσα Επιστημονικό Συνεργάτη με έδρα την ΚΟΡΙΝΘΟ

Duties:

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

 

Qualifications:

Εμπειρία μεγαλύτερη των 3 ετών σε πωλήσεις Προηγούμενη εμπειρία στις πωλήσεις φαρμακευτικών προϊόντων και εμπειρία στο διαβήτη, θα θεωρηθεί επιπλέον προσόν Πτυχίο ΑΕΙ/ΤΕΙ επιθυμητό Ικανότητα επικοινωνίας και ανάπτυξης διαπροσωπικών σχέσεων  Επαγγελματική συνέπεια και ικανότητα εργασίας υπό πίεση Εξαιρετική γνώση Η/Υ

 

Location: ΚΟΡΙΝΘΟΣ, ΕΛΛΑΔΑ

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 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 Digital Marketing Associate to join our Marketing team in our offices in Limassol.

Duties:

The Digital Marketing Associate will have the opportunity to:   Daily follow ups on digital projects and ongoing tasks Assist and coordinate on ad hoc campaigns and new projects Follow up on e-commerce collaborations globally, social media coordination, corporate and brand website administration

 

Qualifications:

Bachelor’s degree in Marketing, Business Management, or related field Minimum 1 year of experience in a similar role Knowledge of marketing digital tools and techniques Good knowledge of SEO and CMS would be considered as an advantage Ability to multitask and meet strict deadlines Excellent communication and interpersonal skills Strong teamwork skills Proficiency knowledge of Microsoft Office

 

Location: 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 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  Ticketing & Travel Associate to join our Ticketing & Travel team in our offices in Limassol .

Duties:

The Ticketing & Travel Associate  will have the opportunity to:   Plan and arrange itineraries, hotels and transfers for in house travellers and/or associates. Administer and check invoices as per quoted prices. Assist, work and provide 24/7 backup to travellers on a rotational basis. Act as a point of contact for the ticketing needs of internal clients and offers efficient service at all times.

 

Qualifications:

University degree or Diploma in Travel & Tourism or other relevant discipline. At least 2 years of service in a similar role. Knowledge of Galileo and/or Amadeus GDS systems, hotel platforms etc. Ability to work collaboratively in a team and prioritize work in a dynamic and fast moving environment. Excellent command of the English language, both written and oral Excellent communication and interpersonal skills.

 

Location: 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 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  Commercial Operations Manager to join our Commercial Operations team in our offices in Limassol .

Duties:

The  Commercial Operations Manager will have the opportunity to:   Take ownership of the Sales data strategy including analytics gathering and reporting, Support management by recognizing past trends and support in forecasting future trends, Define and oversee change management initiatives such as the commercial and operations model and lead generation Develop data driven business models which drive initiatives that are tied to commercial operations strategies, Scale revenue generation through operational excellence using processes to promote best practices for all teams Supervise Sales Force Effectiveness ( SFE ), CRM System Deployment and Integration Optimize Bid Management & RFQ / Tender Support Optimize Order Delivery system Monitors Customer Satisfaction and Service levels to ensure that company standards are met

 

Qualifications:

University degree in Business administration, Mathematics, Statistics, Operations research, Engineering or any other related field At least 5 years of experience  in Business Analytics Ability to work collaboratively in a team and prioritize work in a dynamic and fast moving environment. Analytical & strategic thinking. Excellent command of the English language, both written and oral Excellent communication and interpersonal skills.

 

Location: 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 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)   Medochemie Ltd invites applications from career-oriented professionals for the position of Head of Sales M.E.N.A   This position will be reporting directly to the CEO of the company.

Duties:

Sales Develops and implements the sales strategy of the region. Builds up and supports the business plan of the region by volumes, turnover and budget. Identifies major competitors, potential customers, market trends and developmental opportunities. Decides on variations in pricing, payments and other conditions. Represents the Company and maintains a high level of contact with important clients. Prepares timely information to the Board (Sales report, Stock report, Country report, Sales analysis – primary and secondary sales) or any report needed. Meets and works with partners to discuss sales targets for the following /succeeding year (5-year forecast), marketing plan, etc. New Business Searches and identifies potential new business partners, e.g. expansion of geographic area. Identifies products with potential new partner(s), discuss forecasts, prices, terms of supply, etc. Builds new relationships with new partners Marketing Is responsible for the Region’s general strategy implementation on the market. Develops and implements marketing plans and projects for new and existing products programs. Prepares the proposal for the Region’s products forecast. Is responsible for the execution of the approved marketing budget.   Finance and Accounting Prepares and submits, the Sales & Marketing budget, on an annual basis, for approval of the Board. Monitors all the Region’s expenses and maintains all costs within Budgeted limits. Oversees the preparation of country financial reports required to be submitted to the Board of Directors. Is responsible for the financial KPIs of the region.   Human Resources Manages, supervises, coaches and motivates team.

 

Qualifications:

Bachelor’s degree with at least 15 year of pharmaceutical sales and/or  marketing experience. Academic education in life sciences (medicine, pharmacy, chemistry or other relevant degree) will be considered an important asset. Regional pharma experience in the MENA region is essential. Proven analytical & strategic thinking. Excellent internal and external communicator across multidisciplinary team. Strong project management orientation with the ability to plan, prioritize and manage complex list of projects to completion.   Hands-on and can-do mentality, enjoys working in a team, but can also work autonomously and remotely as an individual. Excellent communication & presentation skills. Excellent English both verbal and writing. frequent traveling abroad is required.

 

Location: Limassol, Cyprus or Cairo, Egypt or Amman, Jordan

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 φαρμακευτική εταιρεία MEDOCHEMIE HELLAS A.E. είναι θυγατρική εταιρεία της MEDOCHEMIE Ltd, που
εξειδικεύεται στην παραγωγή/εμπορία γενοσήμων φαρμάκων και συμπληρωμάτων διατροφής.
Η εταιρεία δραστηριοποιείται σε πάνω από 107 χώρες, έχοντας 13 δικές της μονάδες παραγωγής στην Κύπρο,
την Ολλανδία και την Ασία. Διαθέτει στο χαρτοφυλάκιό της 630 εγκεκριμένα προϊόντα και πάνω από
4.355 εγγραφές προϊόντων παγκοσμίως.
 
H MEDOCHEMIE HELLAS A.E. στοχεύοντας στην περαιτέρω ανάπτυξή της ζητά να προσλάβει άμεσα
Επιστημονικό Συνεργάτη με έδρα την Αττική.

Duties:

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

Qualifications:

• Εμπειρία μεγαλύτερη των 3 ετών σε πωλήσεις
• Προηγούμενη εμπειρία στις πωλήσεις φαρμακευτικών προϊόντων και εμπειρία στο διαβήτη, θα θεωρηθεί επιπλέον προσόν
• Ικανότητα επικοινωνίας και ανάπτυξης διαπροσωπικών σχέσεων
• Επαγγελματική συνέπεια και ικανότητα εργασίας υπό πίεση
• Εξαιρετική γνώση Η/Υ

Location: Aθήνα, Ελλάδα

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 βιογραφικό σημείωμα μέχρι ή να συμπληρώσουν την
online αίτηση παρακάτω
 
 
ΠΡΟΣΟΧΗ:
 
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.

 

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 Δειγματοληπτικών Ελέγχων Παραγωγής με το ακόλουθο ωράριο εργασίας:
 
Απογευματινό  Ωράριο: Δευτέρα- Πέμπτη 14:30-23:00 / Παρασκευή 13:00-19:20

Duties:

• Διενέργεια δειγματοληπτικού ελέγχου καθ' όλη τη διάρκεια της παραγωγής παρτίδων. Τα δείγματα ελέγχονται για να επαληθεύεται η συμμόρφωση με προδιαγραφές όπως η ταυτότητα, η συμμόρφωση των κατασκευαστικών στοιχείων προς τις γραπτές προδιαγραφές, και η εξέταση μόλυνσης.  
• Να παρακολουθεί και να διασφαλίζει την τήρηση των Κανόνων Ασφάλειας καθώς επίσης και των απαιτήσεων των Κανόνων Ορθής Παρασκευαστικής Πρακτικής (GMP), για την διασφάλιση της ποιότητας των προϊόντων.
• Έγκαιρη και σωστή εισαγωγή των απαιτούμενων δεδομένων στα έντυπα και ημερολόγια της συσκευασίας

Qualifications:

• Απολυτήριο λυκείου
• Δίπλωμα Κολεγίου ή Πανεπιστημιακό δίπλωμα θα θεωρηθεί επιπρόσθετο προσόν.
• Βασικές γνώσεις της Αγγλικής γλώσσας
• Πολύ καλή γνώση των Ηλεκτρονικών Υπολογιστών
• Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Λεμεσός, Κύπρος

Benefits
 

• 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
• Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης εαν το επιθυμεις
•  Συμμετοχή στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε 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 βοηθό χημείου για να ενταχθεί στην ομάδα του Χημείου μας στα γραφεία μας στην Λεμεσό.

Duties:

• Οργάνωση και αποθήκευση δειγμάτων σύμφωνα με όλες τις απαιτήσεις ασφάλειας για τη διασφάλιση της ασφάλειας του προσωπικού και της ακεραιότητας του δείγματος
• Προετοιμασία εργαστηριακού εξοπλισμού για   ερευνητικά πειράματα
• Διεξαγωγή αναλύσεων με βάση της απαιτήσεις του    πρωτοκόλλου
• Kαταγραφή δεδομένων στο ηλεκτρονικό αρχείο
• Συντήρηση εργοστασιακού εξοπλισμού
• Τήρηση αρχείων εξοπλισμού και καθημερινών αρχείων καταγραφής εργασιών
• Να ακολουθεί αυστηρά τις διαδικασίες δίνοντας έμφαση στην λεπτομέρια

Qualifications:

• Αποφοιτος/η Λυκείου ή Τεχνικής Σχολής
• Άριστη γνώση ελληνικής και αγγλικής γλώσσας
• Μαθηματικές και μετρητικές δεξιότητες
• Γνώση χειρισμού ηλεκτρονικού υπολογιστή (ms office, email etc)
• Καλές δεξιότητες επικοινωνίας, οργάνωσης και συνεργασίας

Location: Λεμεσός, Κύπρος

Benefits
 

• 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
• Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης εαν το επιθυμεις
•  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.
 

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 Συσκευασίας, για τα ακόλουθο σύστημα βάρδιας:

Κυλιόμενη: Πρωινή/ Απογευματινή/ Νυκτερινή:         
Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)

Duties:

• Συναρμολόγηση, συσκευασία και αποθήκευση φαρμακευτικών σκευασμάτων
  Χειρισμός μηχανημάτων συναρμολόγησης και συσκευασίας

Qualifications:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης ή δίπλωμα/πτυχίο Κολεγίου ή Πανεπιστημίου
  Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
  Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν
  Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Limassol, Cyprus

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
• 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.

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.

Κυλιόμενο Ωράριο:  Πρωινό / Απογευματινό: 7:00 – 15:30 / 14:30 – 23:00  

Duties:

• 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

Qualifications:

• Απόφοιτος Τεχνικής Σχολής ή Τεχνικού κολλεγίου
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Λεμεσός, Κύπρος

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
• 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 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)   Medochemie Ltd invites applications from career-oriented professionals for the position of Sales Manager for our offices in Limassol, Cyprus.

Duties:

Promotion, Sales and Marketing of Pharmaceutical products. Delivery of area sales targets Accountable of area budget management Coaches and develops team through performance development ensuring balance of brand market share and market development priorities Accountable for the execution of the plan managing the effective deployment of resources and integration with the Company’s strategy Identifies and maintains relationships with new and existing customers, meeting agreed sales targets. Monitors and reports on market and competitor activities to support the development of a sustainable and profitable business plan. Strategic planning for existing and future markets. Supports, Monitors and Liaises with local customers, healthcare professionals, importers/distributors, Healthcare authorities and other partners. Sourcing for new Agencies and Distributors, and Business development.

 

Qualifications:

Bachelor’s degree with at least 5 year of pharmaceutical marketing and/or sales experience. Academic education in life sciences (medicine, pharmacy, chemistry or other relevant degree). Proven analytical & strategic thinking. Excellent internal and external communicator across multidisciplinary team. Strong project management orientation with the ability to plan, prioritize and manage complex list of projects to completion. Hands-on and can-do mentality, enjoys working in a team, but can also work autonomously and remotely as an individual. Excellent communication & presentation skills. Excellent English and Greek literature both verbal and writing. Ability to travel abroad.

 

Location: Limassol,Cyprus

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 databse 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).   Medochemie Ltd invites applications from career oriented professionals for the position of Product Manager for our offices in Limassol, Cyprus.

Duties:

Develop deep understanding of all main Therapeutic Area classes of Medochemie portfolio Develop & implement the marketing & communication strategy for each Therapeutic Area. Partner with local marketing teams to collect market and customer insights  for each Therapeutic Area Harmonize value propositions and messaging, clear communication of features and benefits of products Develop pricing strategy and launch sequence plans Create marketing campaigns, marketing materials and customer presentations Responsible to co-ordinate the internal training of teams across regions and ensure readiness for new launches and strategy implementation Create business plans to drive above market growth Generate competitive assessments Key Opinion Leaders management

 

Qualifications:

University degree in a relevant science (Pharmacy, Pharmacology, Chemistry, Biochemistry, Biology, etc) At least 5 years related working experience in the Pharmaceutical Industry Proven analytical & strategic thinking Excellent internal and external communicator across multidisciplinary team Strong project management orientation with the ability to plan, prioritize and manage complex list of projects to completion Hands-on and can-do mentality, enjoys working in a team, but can also work autonomously and remotely as an individual Excellent communication & presentation skills Excellent English and Greek literature both verbal and writing Ability to travel abroad

 

Location: Limassol,Cyprus

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 databse 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 3800 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 invite applications from highly qualified and motivated professionals for the position of Supply Chain Specialist based in Limassol, Cyprus 
 

Duties:

Supply Planning ·   Review and manage Sales Orders generated in the system from Sales Team. ·   Minimize manual process fully operating in the ERP system. ·   In cooperation with Master Scheduling provide the first Estimate Delivery date and communicate to the Customers (Internals / Externals). ·   Communicate to the Customers any deviation vs the final confirmation date. ·   Define and maintain material master data planning /supply chain within ERP. ·   Generate Export documents and book shipments to end Customers Inventory Planning and Control ·   Monitor safety stock and reorder points without hampering the customer service levels ·   Monitor and reduce expired stock in line with Affiliates Team. ·   Monitor backorders and assure on time replenishment. ·   Coordinate inventory allocation and/or transfer during times of supply constrain or in excess ·   Drive inventory optimization based on the safety stock agreed levels. Reporting ·   Create reports on sales/demand, inventory, expiry, for Medochemie Affiliates ·   Analyze and evaluate forecasts accuracy in demand planning system

Qualifications:

• University degree in Supply Chain Management, Chemical Engineering, Industrial Pharmacy or related field
• Minimum 2 years of previous experience in the field of production or supply chain 
• Previous experience in analysis and reporting is a must
• Very good interpersonal skills and analytical thinking
• Able to organize and prioritize work.
• Strong computer literacy
• Fluency in Greek and English language

Location: Limassol, Cyprus

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 databse 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).   Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Assurance Associate (Systems) in our offices in Limassol, Cyprus.

Duties:

Collect and evaluate the necessary information for the preparation of risk assessments related to impurities assessment in pharmaceutical products /materials Prepare / assist the risk assessments Participate in the process of setting mitigation / corrective / preventive actions Identify possible degradation paths and formation of relevant impurities / degradation products and possible inter-molecules reactions in active pharmaceutical substances, manufacturing processes and finished pharmaceutical products Handle cleaning validation activities, including organization, protocol and report preparation, study execution and related deviations handling

 

Qualifications:

Bachelor's degree in Pharmacy or Chemistry, with specialization in organic chemistry.  A post graduate degree will be considered an advantage Related experience in a pharmaceutical industry would be considered an advantage Experience in nitrosamines and elemental impurities evaluation is necessary Fluency in Greek and English language Proficiency with MS office tools (Word, Excel, PowerPoint, etc) Ability to work collaboratively in a team, and prioritize work in a dynamic and fast-moving environment Ability to work in multiple projects Good communication skills (verbal and written) within the department, between departments and with external partners Strong organisational skills and data analysis skills Multi-project handling at once under time pressure

 

Location: Limassol,Cyprus

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 databse 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). Medochemie Ltd invites applications from career-oriented professionals for a position in the areas of Risk, Compliance and Internal Audit.

Duties:

As part of a team and under supervision of Senior Management, responsibilities will include:   Performance of Internal Audits of various departments in Cyprus and abroad Risk analysing and monitoring of the implementation of mitigation actions Assisting in the development and monitoring of the Company’s compliance programme. Monitoring of Key performance indicators Engaging in process improvement projects Assisting in the development of policies and procedures in certain areas for the strengthening of internal controls. Participating in special projects and investigations. Communicating with various departments and external associates. Data collection and analysis. Articulating and presenting findings clearly both verbally and in written reports to the BoD and Senior Management. Travelling to Countries where the Company has operations.

 

Qualifications:

University degree in fields such as Accounting, Economics, Management, Operational Research, Risk, Engineering. Professional Accounting qualification (ACA, ACCA, CPA) and/ or Certified Internal Auditor qualification (CIA) will be considered as an advantage Work experience of at least 5 years in areas such as Internal Audit, Risk and Compliance, Process reengineering, External Audit. Work experience in areas such as manufacturing/ production, logistics, commercial will be considered as an advantage. Project Management experience will be considered as an advantage Proficiency in MS Office including advanced excel skills Knowledge of data analytics tools will be considered as an advantage Excellent knowledge of the Greek and English languages A highly motivated individual who can demonstrate agility, diversity, curiosity, and willingness for continuous learning. A confident individual, able to communicate in a clear and effective manner

 

Location: 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 wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form 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 a Cypriot pharmaceutical company with international exposure offering quality pharmaceutical products to patients in more than 100 countries worldwide. Medochemie manufactures and licenses a wide range of products produced at its 13, GMP-certified manufacturing facilities around the world and divided into more than 10 therapeutic categories.

Medochemie Ltd invites applications from highly qualified and motivated professionals for the position of Regulatory Affairs Associate in our offices in Limassol, Cyprus.
 

Duties:

• To prepare CTD as well as eCTD format dossiers for new products and update the ones for existing products in compliance with the global regulations in force
• To submit and oversee the attainment of Marketing Authorisations according to the company’s commercial strategy and considering the different country-specific requirements
• To submit the necessary lifecycle management activities (renewals and variations) in all territories as necessary to maintain the company’s Marketing Authorisations while enabling the materialisation of the company’s evolving strategy

Qualifications:

• University degree in sciences (e.g. Chemistry, Biochemistry, Biology). A postgraduate degree will be considered an advantage
• Ability to work individually and as part of a team
• Ability to multitask 
• Excellent interpersonal and communication skills
• Analytical Thinking 
• Ability to work under pressure.
• Competency in Microsoft Office applications
• Profficient in the English and Greek language with excellent written and verbal communication skills
Preferred:
 
• At least 2 years of experience within the pharmaceutical industry in the Field of Generic Regulatory Affairs.
• Solid knowledge of Eur.Ph., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs.
• Competency in e-CTD preparation. 

Location: 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 wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form 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 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).   Medochemie Ltd invites applications from  highly qualified and motivated professionals for the position of Quality Control Associate in our offices in Limassol, Cyprus.

Duties:

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)

Qualifications:

University degree in Chemistry, Biochemistry or other relevant field. Post Graduate diploma will be considered an advantage Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, will be considered as an additional asset. Effective verbal and written communication skills Profficient in the English and Greek language with excellent written and verbal communication skills

 
 
 

Location: Limassol, Cyprus

Duties:

• 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
 

Qualifications:

• 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
• 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
• Profficient in the English language with excellent written and verbal communication skills
• Willingness to relocate to Cyprus

Location: 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 wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form 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 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).
 
Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Pharmaceutical Representative in the following areas:  Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.
 

Duties:

o Conducts visits to pharmacies for the proper promotion of the medical products
o Develops and maintain positive clients relationships
o Informs about the new products and seeks their immediate placement in pharmacies
o Controls the stocks of the products
o Solves any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

 

Qualifications:

o Licensed Medical/Pharmaceutical Representatives with at least two years of experience in a similar position
o University degree in Pharmacy, Biology, Chemistry or related field will be considered an advantage
o Profficient in the English language with excellent written and verbal communication skills
o Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: 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 wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form 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 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).

Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Medical Representative in the following areas: Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.

Duties:

• 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

Qualifications:

• Licensed Medical Representatives with at least two years of experience in a similar position.
• University degree in Pharmacy, Biology, Chemistry or related field will be considered an advantage
• Profficient in the English and Greek  language with excellent written and verbal communication skills
• Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: 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 wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form 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 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).

Medochemie Ltd invites applications from career oriented Research and Development Associate based in Limassol, Cyprus. 

Duties:

• 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.

Qualifications:

• University degree in pharmaceutical chemistry or Chemistry.
• Post graduate degree will be considered an advantage.
• Experience in the pharmaceutical industry it will be considered an advantage. 
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment. 
• Very good interpersonal skills, analytical thinking and result orientation.
• Strong computer literacy.
• Fluency in Greek & English language.

Location: Limassol, Cyprus

Benefits   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 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 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).

Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Medical Representative in the following areas:

• Western and Southern provinces, based in Jeddah
• Central province, based in Riyadh 
• Eastern Province, based in Dammam or Khobar 

Duties:

• Conducts visits to doctors and pharmacists (Hospitals and polyclinics) for the proper promotion of the medical products
• Makes sales presentations to multiple decision-makers in order to promote the company’s portfolio of products, within the entrusted territory
• Achieves the sales targets and statutory performance indicators
• Establishes and nurtures client relationships 
• Develops strong relationships with key decision makers and influencers 
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Licensed) 
• Valid specialties accreditation (Practitioner)
• Up to two years of experience in a similar position will be considered as a plus
• Profficient in the English language with excellent written and verbal communication skills
• Very good interpersonal and influence skills, analytical thinking, results orientation.
• Saudi Nationals only

Location: Jeddah, or Riyadh, or Eastern Province, Saudi Arabia

We are offering an attractive remuneration package and challenging opportunity for professional development.
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.