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 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 Senior Specialist in our offices in Athens, GREECE. 

Duties:

• To prepare CTD as well as eCTD format dossiers for new products and update the ones for the existing products in compliance with the global regulations in force. To submit Marketing Authorisation Applications (MAAs) for both European Registration Procedures (DCP/MRP) and non-EU national procedures according to the commercial strategy of Medochemie Ltd, considering the different country specific requirements. 
• To timely submit the necessary lifecycle regulatory activities (renewals and variations) in all territories as necessary so that all Marketing Authorisations are up to date. 

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• At least 5 years of experience in the field of generic product development and regulatory affairs (i.e. knowledge of PhEur, EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs and competency with e-CTD preparation.) 
• 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.
• Fluency in both written and spoken English and computer literacy.

Location: Athens, Greece

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company 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).

Medochemie Ltd invites applications from career oriented professionals for the position of Pharmacovigilance Associate in our offices in Limassol, CYPRUS. Pharmacovigilance is the scientific department of the Company that  deals with the safety of pharmaceutical products.

Duties:

• To collect and manage information on adverse events from various sources and report them to Eudravigilance according to current EU legislation.  
• To regularly perform signal detection activities, as per the Pharmacovigilance system of Medochemie and current EU legislation.
• To maintain the Drug safety information and the Pharmacovigilance system as per internal procedures. 
• To execute a number of task relating to the Quality of the Pharmacovigilance system, including but not limited to trainings, audits, contractual agreements, deviations and quality reviews, as per internal procedures.  

Qualifications:

• University degree in Pharmacy, Medicine or other relevant life science degree. A post graduate degree will be considered an asset.
• Previous experience within the pharmaceutical industry in the field of drug safety and Regulatory Affairs (for generics) will be considered an asset.
• 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.
• Fluency in both written and spoken English.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence. 
 

Medochemie Ltd is an International Pharmaceutical Company 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 Chemical Engineer Professionals. We will employee candidates on the positions of Aseptic Filling Specialist, Senior Specialist or Assistant Manager based on the level of experience.

Duties:

• Coordinate, supervise and control production processes to ensure that products are produced according to the appropriate procedures in order to obtain the required quality.
• Monitor the compliance of the department with the requirements of Good Manufacturing Practice (GMP).
• Carry out the production plan according to the production schedule.
• Effective supervision, coaching, development and monitoring of all production personnel in order to ensure productivity and product quality. 
• Follow and implement new requirements of the Good Manufacturing Practice (GMP). 

Qualifications:

• University Degree in Chemical Engineering, Industrial Pharmacy, Pharmacy or other related field
• At least 5 years of experience in Pharmaceutical Industry
• Good command of the English and Greek language, both written and verbal
• Excellent analytical and technical skills related to this discipline

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company 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 Chemical Engineer Professionals. We will employee candidates on the positions of Specialist, Senior Specialist or Assistant Manager based on the level of experience.   

Duties:

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

Qualifications:

• University Degree in Chemical Engineering, Industrial Pharmacy, Pharmacy or other related field
• Experience specific in Production in an industrial environment is required. Any previous experience in the Pharmaceutical Industry will be considered an important asset
• Good command of the English and Greek language, both written and verbal
• Excellent analytical and technical skills related to this discipline

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company 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 Chemist to join our team based in Company’s offices in Limassol, CYPRUS. We will employee candidates for the levels of Associate or Specialist (based on experience) for our Quality Control and R&D Departments.   

Duties:

Duties for QC:
• To perform physical and chemical analysis on starting materials and finished pharmaceutical dosage forms using a variety of analytical and separation techniques such as High Performance Liquid Chromatography (HPLC),Gas Chromatography (GC), UV/VIS Spectrophotometry, Thin-layer Chromatography (TLC) and IR.
• To carry out stability studies on pharmaceutical products stored under different climatic control conditions  
• Use of statistical tools to monitor trends will be considered as an asset
• To follow all the guideline’s on Good Laboratory Practice (GLP)

Duties for R&D:
• Strong Method development, Method Validation and Method transfer of new analytical methods.
• Experienced in operational knowledge of analytical instrumentation like HPLC, GC, LC/MS, UPLC, TLC, Dissolution apparatus(manual and automated), FTIR and UV-VIS spectrophotometer
• To perform detailed literature searches and review all available literature data for the development of analytical methods and to design new method development if no available procedure can be found in the literature.

Qualifications:

• University degree in Chemistry. 
• Post Graduate or Doctoral degrees will be considered as an additional asset.
• Excellent command of the English language, both written and oral.
• Excellent communication and interpersonal skills.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an international pharmaceutical company 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)
• 0- to two years of experience in a similar position.
• Excellent level of knowledge of the English language.
• 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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company 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 Regulatory Affairs Professionals. We will employee candidates on the positions of Senior Specialists or Specialists based on the level of experience.   

Duties:

• To prepare CTD as well as eCTD format dossiers for new products and update the ones for the existing products in compliance with the global regulations in force. To submit Marketing Authorisation Applications (MAAs) for both European Registration Procedures (DCP/MRP) and non-EU national procedures according to the commercial strategy of Medochemie Ltd, considering the different country specific requirements. 
• To timely submit the necessary lifecycle regulatory activities (renewals and variations) in all territories as necessary so that all Marketing Authorisations are up to date. 

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 within the pharmaceutical industry in the field of generic regulatory affairs. 
• Solid knowledge of PhEur, EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs and competency with e-CTD preparation. 
• 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.
• Fluency in both written and spoken English and computer literacy.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company 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 following positions:

Medical Representatives to cover Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos, for medical promotion
Pharmaceutical Representatives to cover Larnaca/ Ammochostos 

Qualifications:

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

Location: Cyprus

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

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 Παραγωγής, για τα ακόλουθα συστήματα βάρδιας:

Κυλιόμενο ωράριο: Πρωινό/Απογευματινό/ Νυκτερινό:
Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)

Μεταβαλλόμενο ωράριο: προγραμματισμός 8ωρης εργασίας καθόλη τη διάρκεια του 24ωρου:
π.χ. 6:00 – 14:15 ή 8:00 – 16:15 ή 11:00 – 19:15 ή 19:00 – 03:15 ή 05:00 – 13:15 κ.α.

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: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.

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) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν 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 Συσκευασίας, για το 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 και επίβλεψη λειτουργίας μηχανών συσκευασίας φαρμακευτικών σκευασμάτων σύμφωνα με τους Κανόνες Καλής Παρασκευής Φαρμάκων (GMP)
• 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: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.

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) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν 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 υπεύθυνο και συνεργάσιμο άτομο με έδρα τη Λεμεσό στην Κύπρο, για τη θέση Production Shift Associate για εργασία σε πρόγραμμα βάρδιας.

Duties:

• Να εφαρμόζει πλήρως το πρόγραμμα της παραγωγής σύμφωνα με τις οδηγίες του Δ/ντή Παραγωγής.
• 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.
• Χειρισμός,  Ρύθμιση και  Αλλαγή σετ των μηχανών της μονάδας.
• Να προγραμματίζει, συντονίζει, επιβλέπει και γενικά να διοικεί αποτελεσματικά το προσωπικό που εργάζεται στην γραμμή Παραγωγής.
• Να διασφαλίζει  την παραγωγικότητα, την ποιότητα, την υγιεινή και την σωστή συμπεριφορά του προσωπικού.
• Να εντοπίζει και να αναφέρει έγκαιρα στο Τεχνικό τμήμα τυχών μηχανικές βλάβες και να συντονίζει για την έγκαιρη διόρθωση τους.
• Έγκαιρη και σωστή εισαγωγή των απαιτούμενων δεδομένων στα έντυπα και ημερολόγια της παραγωγής.
• Να συνεργάζεται με την ομάδα Συσκευασίας για την αποτελεσματική και ποιοτική συσκευασία των προϊόντων.

Qualifications:

• Κάτοχος πτυχίου Μηχανολόγου Μηχανικού ή Ηλεκτρολόγου Μηχανικού
• Προϋπηρεσία στη Βιομηχανία ή σε Επιστασία προσωπικού θα θεωρηθεί επιπρόσθετο προσόν. 
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.

Location: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών ανάλογα με τα προσόντα και την πείρα.

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) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

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 Specialist in our offices in Limassol, CYPRUS.

Duties:

Provide deviation system oversight
• Review and provide initial criticality assessment for deviations
• Review and approve deviation investigations and corrective action plans
• Review effectiveness of corrective actions

Document Approval
• Prepare, Review and approve Change Proposals and Deviations 
• Prepare, Review and approve SOP’s and other documents
• Prepare, Review and approve Qualification Protocols and reports as needed

Change Control
• Direct the development and implementation of change control to ensure product(s), equipment, test methods, procedures and processes meet appropriate regulatory agency validation requirements, internal company standards and industry current practices.  
• Oversee and review change control processes and procedures, making recommendations for changes and/or improvements. 

General
• Approves protocols, master production batch records, standard operating procedures (SOPs), and sampling plans in support of manufacturing operations.
• Coordinates with Manufacturing to ensure appropriate implementation of changes to processes and systems.
• Reviews and verifies deviation notices generated by the QA Dept during manufacturing, including resolutions and corrective actions.
• Participates in the material review process to evaluate proper disposition of nonconforming materials.
• Provides technical support and oversight through the QA Representatives and directly with the plant and site management, Manufacturing personnel, and other site quality assurance departments, to ensure that the QA needs of the facility and Manufacturing operations are met.
• Prepares and evaluates product trends; participates in annual quality reviews; provides periodic updates and summary reports as needed.
• Support all corporate and regulatory inspections. 
• To evaluate Product Annual Reviews reports.
• Responsible for the execution and coordination of recalls.
• Responsible for handling complaints.
• Involved in implementation of new guidelines

Other
• Develop and administer schedules and performance requirements.
• To be involved in Contract Manufacturing.
• To assist the Company to achieve product compliance as needed.

Qualifications:

University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset. Minimum 3 years of experience in a Quality Assurance Department of an Organization Minimum 5 years of experience in cGMP Environment. Multi project handling at once under time pressure. Excellent command of the English language, both written and oral. Significant knowledge of and experience with FDA/cGMP regulations is required. Advanced project management and technical writing skills is preferred. Prior supervisory, project management, or leadership experience is required. Aseptic Operations Experience will be considered as an additional asset. Ability to work in a team environment and to effectively manage within a matrix organization is required. Committed to relocate to Cyprus. Ability to travel abroad.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence. 

Medochemie Ltd is an International Pharmaceutical Company 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 Technology Transfer Manager for our offices in Limassol, CYPRUS.  

Duties:

• Perform technology transfers of pharmaceutical drug product processes among R&D and Medochemie Production sites, or between Medochemie sites.  
• Manage and mentor the team of experts performing technology transfers.
• Assess processes for gaps, design experiments, write pilot/ batch protocols and batch records, supervise manufacturing batches, assess experimental data, draw scientifically sound conclusions, and write technology transfer reports.
• Perform manufacturing process reviews of processes intended for technology transfer with an eye towards manufacturability, robustness, and validation success.
• Assist in the completion and review of sections of documents needed to complete such transfers.
• Provide scientific trouble shooting having always in mind the quality of products.
• Managing projects to meet Company timelines.

Qualifications:

• University Degree in Pharmacy, Chemistry or Chemical Engineering. 
• Minimum 8 years of experience in cGMP Environment.
• Minimum 8 years industrial experience in a similar position.
• Experience in R&D and production areas will be considered as an additional asset. 
• Good Communication skills.
• Multi project handling at once under time pressure.
• Excellent command of the English language, both written and oral.
• The position will require frequent travelling.
• Committed to relocate to Cyprus.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence. 

Medochemie Ltd is an International Pharmaceutical Company 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 Patent Specialist for our offices in Limassol, CYPRUS.  

Duties:

• To be able to search in available patent data bases in order to explore the status of patent applications, litigations etc in European and non- European territories.
• To be able to review, analyze and advice on patents and prepare consolidated patent reports. 
• To be in a position to assess and conclude on finished dosage formulations and active substances’ synthetic schemes towards any valid patents for a specific product.

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry). A post graduate degree will be considered an asset.
• 10 years of experience within the pharmaceutical industry and specifically as patent officer/ expert in generics.
• Ability to work collaboratively in a team.
• Excellent level of knowledge in written and spoken English and computer literacy.
• Willingness to travel frequently or preferably relocate to Cyprus.

Location: Limassol, CYPRUS

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/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence. 

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 Φύλακα - Θυρωρού:

Ωράριο: Πρωινό/ Απογευματινό/ Νυκτερινό:         
Δευτέρα- Κυριακή: 07:00-15:00/ 15:00-23:00/ 23:00-07:00 

Duties:

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

Qualifications:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης
• Απαραίτητη Άδεια άσκησης του επαγγέλματος Ιδιώτη Φύλακα
• Τουλάχιστον 2 χρόνια προϋπηρεσία
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.

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) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

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 Pharmacovigilance Specialist in our offices in Limassol, CYPRUS. Pharmacovigilance is the scientific department of the Company that takes care of the safety of pharmaceutical products.

Duties:

• To collect and manage information on adverse events from various sources and report them to authorities according to current EU legislation. 
• To perform a number of duties related to Pharmacovigilance, including but not limited to update of drug safety information and signal management, as these are defined by the Pharmacovigilance System of Medochemie and current EU legislation.
• To execute administrative tasks relating to the maintenance of the Pharmacovigilance system and its Quality System, according to written procedures.

Qualifications:

• University degree in Pharmacy or Medicine. A post graduate degree will be considered an asset.
• Minimum ten years of clinical experience.
• 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.
• Fluency in both written and spoken English.
• Committed to relocate to Cyprus.

Location: Limassol, CYPRUS

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

Medochemie Ltd is an International Pharmaceutical Company 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 Formulation Associate for our offices in Limassol, CYPRUS.

Duties:

• To prepare trial batches and to determine the formulation percentage composition of pharmaceutical dosage forms at the Production Formulation Development Laboratory (PFDL)
• To develop new formulations following the company’s new product portfolio and development plans
• To prepare as many formulations as necessary to obtain a stable product essentially similar in vitro with the reference product
• To study the reference product and be able to develop a generic with similar in vitro behavior
• To study the literature of the product and know its pharmaceutical characteristics
• To follow Regulatory Affairs requirements and current European and WHO guidelines related to the development pharmaceutics section and stability guidelines
• To develop products which will be easy to produce in the company’s premises with current equipment

Qualifications:

• University Degree in Pharmacy or related field
• Excellent Pharmaceutical and Technology skills related to this discipline
• Multi project handling at once under time pressure
• Excellent command of the English language, both written and oral
• 3-5 years industrial experience in a similar position involving the above duties
• Committed to relocate to Cyprus

Location: Limassol, Cyprus

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 apply online.
 

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

All applications will be treated in strict confidence.