Careers

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)

Ευέλικτο 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.

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 and Marketing Manager with a proven experience in the OTC/FS division for our office in Prague, Czech Republic. 

Duties:

• Contributes in the design and implementation of the business plan and is responsible for its achievement in terms of volume, turnover and budget in accordance with the Company's goals and objectives
• Contributes in the design and implementation of the marketing plan in accordance with the Company's objectives
• Identifies growth opportunities and proposes strategies and action plan in order to develop and promote the Company's products
• Ensures the achievement of the annual sales objectives as well as monitoring and improving our client portfolio.
• Responsible for the performance, evaluation and development of the sales and marketing team

Qualifications:

• University degree in Medicine, Pharmacy or other related discipline
• Master’s degree in Management, Marketing or Business related subject will be considered an advantage 
• At leats five (5) years previous work experience in the pharmaceutical market at a similar position is essential 
• Fluent in Czech and English languages, both written and spoken 
• Computer literacy 
• In-depth knowledge of the local market
• Very good organisational and interpersonal skills
• Self-motivated and results oriented professional 

Location: Prague, Czech Republic

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 Production Specialist in our offices in Limassol, CYPRUS.

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 or other related field
• Minimum 3 years of experience in an industrial environment
• 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 professionals for the position of Senior Production Specialist in our offices in Limassol, CYPRUS.
 

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 or other related field
• Minimum 5 years of experience in the 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 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 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.
• Experience in the pharmaceutical industry will be considered as 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 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 position of Regulatory Affairs Specialist in our offices in Limassol, CYPRUS.

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 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: 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 Head of Process Validation for our offices in Limassol, CYPRUS. 

Duties:

• To coordinate preparation of process validation protocols, final reports for and Holding Times Studies for all the Company’s facilities.
• To coordinate execution of  process validation protocols according to the Master Plan
• To review protocols and reports prepared by other members of the Team.
• To ensure that the Process Validation protocols have been executed and completed as per requirements and all the deviations have been recorded accordingly. 
• To write Standard Operating Procedures for the Process Validation Department.
• To provide information to other Departments of the Company when needed.
• To write and follow up Validation Master Plan for Process Validation. 
• To prepare transfer protocols and reports for trials and scale ups of new products and charts with suggested limits of IPC tests. 
• To assist with Risk Management projects. 

Qualifications:

• University degree in Pharmacy, Chemical Engineering or other relevant discipline. A post graduate degree will be considered an asset.
• At least 5 years of experience in Process Validation in a Quality Assurance Organization.
• At least 10 years of experience in cGMP Environment.
• Understanding of cGMP requirements and other FDA/EU regulatory requirements associated with manufacture of pharmaceutical products and associated equipment and facilities is essential.
• Knowledge of statistics and their application to such aspects as process sampling and data trends analysis.
• Practical experience with quality risk management and risk based validation approaches.
• Excellent command of the English language, both written and oral.
• Significant knowledge of and experience with FDA/cGMP regulations is required. 

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.

Qualifications:

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

Location: Crete, Greece

Η Εταιρεία προσφέρει:

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

Η MEDOCHEMIE HELLAS A.E., είναι μία από τις ταχύτερα αναπτυσσόμενες εταιρείες γενοσήμων στην Ελλάδα και θυγατρική της παγκόσμιας φαρμακευτικής εταιρείας MEDOCHEMIE Ltd, η οποία εξειδικεύεται στην ανάπτυξη, παραγωγή και διάθεση γενόσημων θεραπειών για πάνω από 40 χρόνια, διαθέτοντας συνολικά 22 γραφεία ανά τον κόσμο. Το ανθρώπινό της δυναμικό αριθμεί πάνω από 1.650 υψηλής εξειδίκευσης και ικανότητας επαγγελματίες, έχει στην κατοχή της 4.500 άδειες κυκλοφορίας και διαθέτει 13 σύγχρονες εργοστασιακές μονάδες στην Κύπρο, την Ολλανδία και το Βιετνάμ. Η δραστηριότητα της εκτείνεται σε περισσότερες από 107 χώρες παρέχοντας θεραπευτικές λύσεις σε πάνω από 300.000.000 ανθρώπους.

H MEDOCHEMIE HELLAS A.E. στοχεύοντας στην περαιτέρω ανάπτυξή της αναζητά να προσλάβει άμεσα Επιστημονικούς Συνεργάτες με έδρα τον Βόλο.

Qualifications:

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

Location: Volos, Greece

Η Εταιρεία προσφέρει:

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

Η MEDOCHEMIE HELLAS A.E., είναι μία από τις ταχύτερα αναπτυσσόμενες εταιρείες γενοσήμων στην Ελλάδα και θυγατρική της παγκόσμιας φαρμακευτικής εταιρείας MEDOCHEMIE Ltd, η οποία εξειδικεύεται στην ανάπτυξη, παραγωγή και διάθεση γενόσημων θεραπειών για πάνω από 40 χρόνια, διαθέτοντας συνολικά 22 γραφεία ανά τον κόσμο. Το ανθρώπινό της δυναμικό αριθμεί πάνω από 1.650 υψηλής εξειδίκευσης και ικανότητας επαγγελματίες, έχει στην κατοχή της 4.500 άδειες κυκλοφορίας και διαθέτει 13 σύγχρονες εργοστασιακές μονάδες στην Κύπρο, την Ολλανδία και το Βιετνάμ. Η δραστηριότητα της εκτείνεται σε περισσότερες από 107 χώρες παρέχοντας θεραπευτικές λύσεις σε πάνω από 300.000.000 ανθρώπους.

H MEDOCHEMIE HELLAS A.E. στοχεύοντας στην περαιτέρω ανάπτυξή της, αναζητά να προσλάβει άμεσα Επιστημονικούς Συνεργάτες με έδρα την Αθήνα.

Qualifications:

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

Location: Athens, Greece

Η Εταιρεία προσφέρει:

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

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 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.

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 Engineering Associate.

Duties:

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

Qualifications:

• Κάτοχος πτυχίου Μηχανολόγου Μηχανικού ή Ηλεκτρολόγου Μηχανικού
• Προηγούμενη πείρα στη συντήρηση τεχνικού εξοπλισμού και βιομηχανικών εγκαταστάσεων θα θεωρηθεί επιπρόσθετο προσόν 
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.
• Πιθανή εργασία σε πρόγραμμα βάρδιας

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.

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.

Qualifications:

• University degree in Chemistry or other relevant discipline.
• Post Graduates or Doctoral degrees will be considered as an additional asset.
• Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, 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 applications from career oriented professionals for the position of Validation Engineering Specialist for our offices in Limassol, Cyprus. 

Duties:

• To execute the revalidation protocols for the existing machines/ systems at the predefined time frame.
• To prepare and execute the Installation, Operation and Performance Qualification Protocols for the new machines/systems.
• To prepare and execute the Change Control Qualification Protocols.
• Responsible to implement the Engineering Validation schedule.

Qualifications:

• University degree in Mechanical Engineering or Electrical Engineering.
• Minimum 5 years of experience in cGMP Environment.
• Minimum 5 years industrial experience in a similar position involving the above duties. 
• 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 applications from career oriented professionals for the position of Process Validation Senior Specialist for our offices in Limassol, CYPRUS. 

Duties:

• To prepare protocols, final reports for Process Validation and Holding Times Studies for all the Company’s facilities
• To execute process validation protocols according to the Master Plan
• To review protocols and reports prepared by other members of the Team
• To ensure that the Process Validation protocols have been executed and completed as per requirements and all the deviations have been recorded accordingly
• To write Standard Operating Procedures for the Process Validation Department
• To provide information to other Departments of the Company when needed
• To write and follow up Validation Master Plan for Process Validation
• To prepare transfer protocols and reports for trials and scale ups of new products and charts with suggested limits of IPC tests
• To assist with Risk Management projects

Qualifications:

• University degree in Pharmacy, Chemical Engineering or other relevant discipline. A post graduate degree will be considered an asset
• At least 5 years of experience in Process Validation in a Quality Assurance Organization
• At least 10 years of experience in cGMP Environment
• Understanding of cGMP requirements and other FDA/EU regulatory requirements associated with manufacture of pharmaceutical products and associated equipment and facilities is essential
• Knowledge of statistics and their application to such aspects as process sampling and data trends analysis
• Practical experience with quality risk management and risk based validation approaches
• Excellent command of the English language, both written and oral
• Significant knowledge of and experience with FDA/cGMP regulations is required

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 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. 

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 Financial Manager for our offices in Prague, Czech Republic. 

Duties:

General responsibilities:
Provide support to the company, through maintaining the financial records and information analyses (e.g. current processes, actual performance vs budget and prior year, etc.), preparation of operational data/analyses for publication to various constituents throughout company (Management, Sales, Product Management, Operations, etc.) who rely on/benefit from the information to make informed business decisions. Primary responsibilities will include preparation and maintenance of financial records, assisting Operations team in the Monthly Operations Review, identification of areas for cost reductions and operational improvements, annual budget process, periodic forecasting, and periodic analysis of operations performance. 

Specific Responsibilities:
• The successful candidate will report to HQ Finance team and to the Country Manager.
• Key responsibilities of the positon include amongst other to: 
• Prepare, maintain, examine, and analyse accounting records, financial statements, and other financial reports to assess accuracy, completeness, and conformance to reporting and procedural standards. 
• Prepare monthly analysis of sales and operational expenses against prior year and budget, providing explanations and business solutions to help manage business risks. 
• Analyse financial performance against key business metrics and document pertinent financial highlights that will enable management to determine progress against budgets. 
• Identify, investigate, and analyse potential operational improvement. As appropriate, based on findings make proposals for operational changes (policy, procedures, processes, controls etc.) 
• Participate in the strategic review and implementation of operational structure of Medochemie in Czech Republic.
• Manage, safeguard and control company’s financial resources ensuring that they are properly used for company’s purposes. 
• Understand and follow company policies and procedures. 
• Perform all other duties as assigned and required. 
• Maintain accurate cash flow management. 
• Coordinate the annual external audit. 
• Liaise with banks, customers and external advisors.  

Qualifications:

• Bachelor’s/ Master degree in business, accounting or related discipline.   
• 3-5 years of experience in a similar position, experience with operations preferred. 
• Preparation and submission of VAT forms and comply with any other tax requirement. 
• Strong experience in income statement analysis. 
• Experience in working with ERP system and Business Intelligence systems will be a plus. 
• Self- motivated with strong analytical, problem solving skills and initiative to achieve desired outcomes. 
• Strong prioritization skills handling multiple priorities. 
• Excellent verbal and written communication skills. 
• English language proficient (both written and verbal). 
• Have a flare for numbers, work well with people, and aggressively anticipate impacts of workload/issues. 
• Adherence to team deadlines. 
• Proficiency in Microsoft office. 

Location: Prague, Czech Republic

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 Quality Assurance Assistant for our offices in Limassol, CYPRUS.

Duties:

• Assists the team in preparation of reports, presentations and QA materials.

Qualifications:

• Τwo or three years higher education degree
• Good command of the English language, both written and verbal
• Excellent knowledge of Microsoft Office
• Professional approach to work and excellent character

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 Quality Assurance Associate in our offices in Limassol, CYPRUS.

Duties:

To prepare and review Standard Operating Procedures and other documents. To prepare and review Change Proposals and deviations. To review Batch records. To review and provide initial criticality assessment for deviations. To review and perform deviation investigations and corrective action plans. To review the effectiveness of corrective actions To assist in self inspections and perform the follow up. To assist in external inspections. To ensure that: The monitoring and control of the manufacturing environment is carried out. The hygiene rules are followed by the personnel. Training programs are carried out. Gowning procedures are followed. All validations are carried out. To oversee and review change control processes and procedures, making recommendations for changes and/or improvements.

 

Qualifications:

• University degree in Pharmacy or Chemical Engineering. A post graduate degree will be considered an asset.
• Multi project handling at once under time pressure.
• Excellent command of the English language, both written and oral.
• Advanced project management and technical writing skills is preferred.
• Experience in the field of pharmaceutical industry will be considered as an asset.
• Ability to work in a team environment and proritize work in a dynamic and fast moving environment.

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. 

Duties:

Collaborating with Quality, Engineering and Manufacturing to ensure robust process/methods transfer. Provide technical leadership for the tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing at all locations. The following tasks are supported from this function: Directs and supports activities related to New Products introduction as it relates to Site issues, capacities, and capabilities. Directs and supports activities related to successful manufacture of new product or existing product stability and validation batches through coordination and communication of the involved departments. Plans work schedules and personnel to accomplish the required duties in a timely manner according to approved schedules. Participates in various new product team meetings and committee meetings as required to support the process and or project. Develops and recommends the product validation matrix. Cooperate with QC excellence to assure the needed analytical method transfer. Cooperate with Regulatory department to assure the provision of needed documentation for registration. Identifies risk involved in manufacturing a product and develop/review the validation protocol to qualify the new product or modified existing product. Keeps abreast of cGMP requirements. Identifies and implements process improvements designed to improve efficiency and enhance product quality.

Qualifications:

University degree in a relevant science (Pharmacy, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Ability to work with cross-functional team and global team. Good knowledge in Project management. Excellent command of the English language, both written and oral. 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 career-oriented professionals to apply for the position of Manufacturing Continuous Improvement Manager for our offices in Limassol, CYPRUS.

Duties:

Continuous improvement Provides Continuous Improvement support to the sites. These are larger individual projects to improve OEE, Deviations, Yield, etc. Provides Project support. This position will be the primary interface for technical transfers, engineering projects and similar activities. This role will provide support for the projects, especially for time intensive and major projects. Ensure efficient and effective operation by creating a proactive environment, developing & monitoring metrics, and communicating with both team members and support functions about operations performance. Ensure the compliance with all regulatory requirements and good documentation practices to provide a safe, quality, and effective product. Leads root cause analysis for Continuous improvement and definition of solutions for key defects. Evaluates diagnose and resolves technical issues and/or process problems based on data analysis. Bring together cross-disciplinary teams when working on complex or recurring problems or pursuing business opportunities. Access and uses other experts when appropriate. Quality management review process support​   Organize periodic management review per region and at group level, with the involvement of senior management, of the operation of the Pharmaceutical Quality System to identify opportunities for continual improvement of products, processes and the system itself.  Establish the right KPIs for an effective QMR. Coordinate Heads of departments to participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement”. Ensure continuing suitability and effectiveness of the Quality Management System and GMP compliance through participation in Management Review.

Qualifications:

University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Chemical Engineering, etc). A post graduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Understanding of cGMP requirements and other FDA/EU regulatory requirements associated with manufacture of pharmaceutical products and associated equipment and facilities is essential. Familiarity with electronic QA systems /database Excellent command of the English language, both written and oral. 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 career-oriented professionals for the position of Process Engineering & Statistics Expert for our offices in Limassol, CYPRUS.
 

Duties:

Working with site process owners, assure the proper transfer of technical knowledge and documentation to support new products, process changes and manufacturing sites. Collaborating with Quality, Engineering and Manufacturing to ensure robust process/validation protocols and reports. Provide process engineering expertise to assure the manufacturing process remains fully validated through process change evaluations and implementations. Provide technical leadership as required during start-up efforts of new equipment or processes in manufacturing. Provide technical leadership for the tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing at all locations. Identify opportunities to implement operational excellence and continuous improvement. Assist the technical operations team to resolve any issues related to production. The following tasks are supported from this function: Support organization, implementation and maintenance of production process flow. Develop working instructions, working standards and process documents, and ensure they are followed. Improve continually existing operation, for increased quality, productivity, efficiency and cost savings. Investigate operational problems affecting production and reporting and recommending solutions. Provide manufacturing data i.e. production control charts, calculate process capability, to improve the process and monitor and measure progress to target. Identify ways to reduce production costs through recommendations – i.e. new process equipment.

Qualifications:

University degree in a relevant science (Pharmacy, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Ability to work with cross-functional team and global team. Good knowledge in Project management Excellent command of the English language, both written and oral. Committed to relocate to Cyprus

Location: LIMASSOL, CYPRUS

Duties:

Establish the Risk Management process/ function within the Company. Coordinate risk management process as needed. Ensure overall effectiveness of risk management process at site. Update / administer the Risk Management database. Develop and implement various techniques for proactive risk identification. Ensure good risk description and scoring as per standards. Ensure risk owners & mitigation leaders are assigned for all risks. Ensure availability of mitigation plans for the identified risks. Ensure training is imparted to all the relevant stakeholders on Risk Management process by providing training materials and actual trainings. Support risk management process for projects in co-ordination with project manager / leader.

Qualifications:

University degree in a relevant science (Pharmacy, Chemistry, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Knowledge on basics of risk management and ICH Q9 principles. Knowledge on risk management tools & templates. Deployment of an appropriate methodology to conduct risk assessments. Ability to work with cross-functional team and global team. Basic knowledge in Project management. Experience in handle tasks independently. Excellent command of the English language, both written and oral. Committed to relocate to Cyprus.

Location: LIMASSOL, CYPRUS

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 Medical Representative (Number of the positions: 3)

Duties:

• Conducts visits to doctors and pharmacies 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 promotional indicators
• Establishes and nurtures client relationships
• Develops strong relationships with key decision makers
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Licensed as a practitioner)
• 0 to 2 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 National.

Location: Jeddah & Al-Madinah, Saudi Arabia Riyadh (central Province), Saudi Arabia Al-Qassim, 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 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 Senior Formulation Associate for our offices in Limassol, CYPRUS

Duties:

• To prepare trial batches and to determine the formulation percentage composition of pharmaceuticaldosage 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 reproduce 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 guidelines and WHO 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.
• To produce scale up batches that compare to the newly developed product.
• To be able to co-ordinate a team of scientists in order to achieve the company targets.

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
• Minimum 7 years’ industrial experience in a similar position involving the above duties
• Proven record of leading scientific teams comprised of highly specialised individuals
• 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.

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.