Καριέρα

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

We invite applications from highly qualified and motivated professionals for the position of HR Specialist based in Limassol, Cyprus.  
 

Καθήκοντα:

•    Acts as first point of contact for HR requests
•    Assists in the development and implementation of policies and procedures
•    Maintains human resource information system records 
•    Performs data analysis and report preparation-incorporating determinations into recommendations
•    Performs compensation and benefits administration and reporting. 
•    Assists in talent acquisition and recruitment processes 
•    Provides HR project support for internal projects
•    Coordinates employee development plans and performance management
•    Provides efficient and effective HR assistance and service to overseas offices  
•    Assists with all internal and external HR-related matters
 

Προσόντα:

•    University Degree in Human Resources Management or any other related discipline
•    Minimum 3 years of experience in a similar role 
•    Strong knowledge on HR processes and operations
•    Hands-on experience with Human Resources Information Systems
•    Solid understanding of labor legislation
•    Strong computer literacy; advance excel user 
•    Fluency in Greek and English language 
•    Maintains confidentiality and professional demeanour
•    Very good interpersonal skills and problem-solving abilities
•    Desire to work as a team with a results driven approach

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. 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:
 

• Ωράριο: Πρωινό/ Απογευματινό/ Νυκτερινό:         

Καθήκοντα:

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

Προσόντα:

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

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13^ο μισθό, 14^ο 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 το βιογραφικό σας σημείωμα στην ακόλουθη ηλεκτρονική διεύθυνση:
 
http://www.medochemie.com/MainMenu/Careers.aspx
 
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 Επιστάτης/τρια Συσκευασίας με το ακόλουθο σύστημα βάρδιας:
 
Κυλιόμενο: Πρωινή/ Απογευματινή/ Νυκτερινή: Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)
 

Καθήκοντα:

 
• Να εφαρμόζει πλήρως το πρόγραμμα της συσκευασίας 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.
• Να προγραμματίζει, συντονίζει, επιβλέπει και να διοικεί αποτελεσματικά το προσωπικό που εργάζεται στην γραμμή Συσκευασίας.
• 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 συσκευασίας.
• Να συνεργάζεται με την ομάδα Παραγωγής για την αποτελεσματική και ποιοτική συσκευασία των προϊόντων.

Προσόντα:

• Απολυτήριο λυκείου
• Δίπλωμα Κολεγίου ή Πανεπιστημιακό δίπλωμα θα θεωρηθεί επιπρόσθετο προσόν.
• Προϋπηρεσία στην Επιστασία/διοίκηση προσωπικού θα θεωρηθεί επιπρόσθετο προσόν.
• Καλή γνώση της Αγγλικής γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13^ο 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 το βιογραφικό σας σημείωμα στην ακόλουθη ηλεκτρονική διεύθυνση:
 
https://www.medochemie.com/Careers.aspx
 
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 Regulatory Affairs Specialist in our offices in Athens, GREECE.

Καθήκοντα:

• Be responsible for the CMC compilation of dossiers for new products and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force.
• Submit Marketing Authorisation Applications (MAAs) and follow up till approval mainly for European Registration Procedures (DCP/MRP) according to the company’s strategy. 
•  Successfully maintain dossiers’ and MA’s lifecycle (variations & renewals) in all territories as necessary so that the MAs are up to date.
• Participate in developing Regulatory strategies within the department, interact and negotiate with competent Authorities and maintain close working relationship with internal stakeholders (e.g. QA, QC, production, commercial). 

Προσόντα:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• 3 to 5 years experience in the pharmaceutical sector, in the field of generic product development and Regulatory Affairs.
• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines and competency with e-CTD preparation
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment. 
• Strong communication, influencing and problem resolution skills.
• Ability to be adaptive to change, to multitask and give attention to detail.
• Very good interpersonal skills, analytical thinking and result orientation.
• Fluency in Greek and English (written and spoken) and computer literacy.  Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

Τοποθεσία: 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 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.
 

Καθήκοντα:

Εκτέλεση προληπτικής συντήρησης των μηχανήματων παραγωγής και των συστημάτων υποστήριξης (κλιματισμός, θέρμανση, εξαερισμός, συμπιεσμένος αέρας)   Εκτέλεση επισκευών/ επιδιόρθωση βλαβών  των μηχανήματων παραγωγής και των συστημάτων υποστήριξης υπό την καθοδήγηση του Μηχανολόγου Συντήρησης. Εκτέλεση ελέγχων και παρακολούθηση  των συστημάτων κλιματισμού, θέρμανσης και εξαερισμού Λειτουργία και έλεγχος των συστημάτων επεξεργασίας νερού. Λειτουργία και έλεγχος των συστημάτων παραγωγής και διανομής ατμού.

 

Προσόντα:

Απόφοιτος Τεχνικής Σχολής στον κλάδο Μηχανολογίας, στην κατεύθυνση  Μηχανικής αυτοκινήτων ή άλλων σχετικών προσόντων. Πολύ καλή γνώση στην εφαρμογή προγραμμάτων συντήρησης καθώς και στην επισκευή και επιδιόρθωση μηχανημάτων και τεχνικού εξοπλισμού. Εμπειρία στην επίλυση τεχνικών προβλημάτων. Προϋπηρεσία στη Βιομηχανία θα θεωρηθεί επιπρόσθετο προσόν. Γνώση της Αγγλικής γλώσσας. Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα.

 

Τοποθεσία: Λεμεσός, Κύπρος

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο 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 τμήματος Καθαριότητας.
 

Καθήκοντα:

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

Προσόντα:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης
• Βασικές γνώσεις της Αγγλικής γλώσσας
• 2 χρόνια προϋπηρεσία σε παρόμοια θέση
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Τοποθεσία: Λεμεσός, Κύπρος

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13^ο μισθό, 14^ο 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 Control (QC) Technician for our offices in Limassol, Cyprus.

Καθήκοντα:

• Receive, label and store samples to be tested
• Perform analysis and testing of products for product approval and release
• Report data and primary results; gather all necessary documentation
• Maintain equipment and assist in ordering laboratory supplies.
• Keep the working area clean and tidy, as per the Laboratory Hygiene and Safety Guidelines

Προσόντα:

• School leaving certificate; college diploma will be considered as advantage
• Excellent command of the Greek and English language, both written and oral
• Excellent knowledge of Microsoft Office
• Excellent communication and interpersonal skills
• Multi project handling at once under time pressure
• Experience in the field of pharmaceutical industry will be considered as advantage

Τοποθεσία: 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 Engineering Packing Manager in our offices in Limassol, CYPRUS.

Καθήκοντα:

• Define, develop, lead and implement packaging designs across product lines in collaboration with the product development teams. 
• Able to oversee all packaging engineering activities related to new product development
• Work directly with Production/Packaging Managers to develop new packaging designs that are cost effective and still meet aggressive time line requirements
• Provide continuous engineering support for packaging on existing products and new products
• Reviews and approves all packaging/labelling specifications and other technical documentation for assigned product lines.
• Support Operations in optimizing packaging related equipment and processes in our manufacturing facilities
• Work with suppliers to optimize packaging design and processes; document and validate changes under the internal quality system
• Attend technical reviews with cross-functional leadership and development teams to provide recommendation on effective packaging/labelling solutions
• Lead and provide packaging engineering expertise on technical projects (e.g. moulds development, introduction of new packaging materials and/or technologies). 
• Subject matter expert on specific assignments (e.g. Solids packaging in blisters, Shrink sleeving technology, deployment of Child-Resistant Senior Friendly Packaging solutions, transportation studies, member of The Company Corporate Pharmaceutical Serialisation, Traceability and TE Team). 
• Provide technical packaging support to Operations (e.g. authoring of packaging components technical specifications, troubleshooting packaging quality issues to improve pack lines efficiency, perform new packaging tooling evaluation, active involvement in new equipment FAT/SAT execution & Performance Qualification of new products in the packaging lines, participation in packaging-related Risk Assessment sessions). 
• Perform audits and evaluation of packaging materials manufacturers/suppliers. 

Προσόντα:

• Bachelor's Degree in engineering or any other related field 
• Minimum 10 years’ experience in packaging engineering in the pharmaceutical industry; /consumer goods/cosmetics industries.
• In-depth knowledge of packaging systems and GMP standards in pharmaceutical industry
• In-depth knowledge of primary and secondary packaging of pharmaceutical drug products
• Experience in graphics, structural and retail package design and deployment required
• Advanced project management and technical writing skills is preferred.
• Strong computer literacy skills
• Fluency in Greek and English language

Τοποθεσία: Limassol, CYPRUS

We are offering an attractive remuneration package based on the candidate’s experience and relevant qualifications as well as great opportunities 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 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).
We invite applications from highly qualified and motivated professionals for the position of Supply Chain Specialist based in Limassol, Cyprus.  

Καθήκοντα:

• Review and manage Sales Orders generated in the system from Sales Team. 
• In cooperation with Master Scheduling provide the first Estimate Delivery date and communicate to the Customers.  
• Define and maintain material master data planning. 
• Monitor safety stock and reorder points. 
• Monitor backorders and assure on time replenishment. 
• Coordinate inventory allocation 
• Create reports on sales/demand, inventory, expiry etc
• Analyze and evaluate forecasts accuracy in demand planning system 
• Drive inventory optimization based on the safety stock agreed levels. 

Προσόντα:

• University degree in Engineering, Mathematics, Operational Research or any other related field. A post graduate degree will be considered an asset.
• Minimum 2 years of previous experience in the field of production or supply chain 
• Previous experience in analysis and reporting is a must
• Very good interpersonal skills and analytical thinking
• Able to organize and prioritize work. 
• Strong computer literacy
• Fluency in Greek and English language 

Τοποθεσία: Limassol, CYPRUS

We are offering an attractive remuneration package based on the candidate’s experience and relevant qualifications as well as great opportunities 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 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 a Cypriot pharmaceutical company with international exposure offering quality pharmaceutical products to patients in more than 100 countries worldwide. Medochemie manufactures and licenses a wide range of products produced at its 13, GMP-certified manufacturing facilities around the world and divided into more than 10 therapeutic categories.
Medochemie Ltd invites applications from career-oriented Regulatory Affairs Professionals.

Καθήκοντα:

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

Προσόντα:

Required:
• University degree in sciences (e.g. Chemistry, Biochemistry, Biology). A postgraduate degree will be considered an advantage. asset.
• Ability to work both individually and as part of a team, as well as prioritise work in a dynamic and fast-moving environment. 
• Excellent interpersonal skills, analytical thinking and ability to work under pressure.
• Competency in Microsoft Office applications.
• Fluency in both written and spoken English.
Preferred:
• At least 3 years of experience within the pharmaceutical industry in the Field of Generic Regulatory affairs.
• Solid knowledge of Eur.Ph., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs.
• Competency in e-CTD preparation. 

Τοποθεσία: Limassol, CYPRUS

We are offering an attractive remuneration package based on the candidate’s experience and relevant qualifications as well as great opportunities 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 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.

Καθήκοντα:

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

Προσόντα:

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

Τοποθεσία: 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 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
We invite applications from highly qualified and motivated professionals for the position of R&D Associate based in Limassol, Cyprus. 

Καθήκοντα:

• Be responsible for the raw materials sourcing for under development products, by contacting with a variety of external stakeholders. 
• Conduct a preliminary and limited quality evaluation of the raw material used for R&D purposes in accordance with the current guidelines in force.
• Apply basic regulatory knowledge under which the medical products are governed.
• Compile consolidated summaries and provide required reports throughout the development of each products in support to the R&D team.
• Support other departments related to the R&D functions and operations when this is required. 

Προσόντα:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Experience in the pharmaceutical industry it will be considered an advantage. 
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment. 
• Very good interpersonal skills, analytical thinking and result orientation.
• Strong computer literacy
• Fluency in English language 

Τοποθεσία: 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. 
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).
We invite applications from highly qualified and motivated professionals for the position of R&D Senior Patent Specialist based in Limassol, Cyprus.  

Καθήκοντα:

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

Προσόντα:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Minimum of 4 years’ experience as patent specialist in generic medicines is a must
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment
• Very good interpersonal skills, analytical thinking and result orientation
• Strong computer literacy
• Fluency in English language
• Committed to relocate to Cyprus

Τοποθεσία: 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. 
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 Software Engineer Specialist/Senior Specialist for our offices in Limassol, CYPRUS. 
 

Καθήκοντα:

• Execute/Monitor the full software development life cycle (SDLC) for new platforms/tools
• Prepare the specifications and determine operational feasibility
• Integrate software components into a fully functional software system
• Document and maintain software functionality
• Troubleshoot, debug and upgrade existing systems
• Deploy software and evaluate user feedback
• Manage projects and coordinate with vendors to ensure the on-time delivery and quality of technology projects
• Track and monitor project progress and escalate issues to appropriate stakeholders
• Continually identify, prioritize and mitigate project risks and issues
• Manage procurement and contract management processes when applicable
• Forecast internal resource capacity by tracking the progress of projects across the portfolio
• Estimate project costs and manage the project budget 

Προσόντα:

• BSc degree in Computer Science, Engineering or relevant field
• 5+ years of proven work experience as a Software Engineer or Software Developer. Data Analytics experience will be considered as an advantage
• Experience in designing and developing interactive applications
• Experience in designing and developing interfaces between systems. Experience in designing and developing Application Programming Interfaces (API) will be considered as an advantage
• Ability to develop software in Java, ASP.NET, C++ or other programming languages
• Excellent knowledge of relational databases, SQL and NoSQL technologies
• Experience developing web applications (PHP, Python)
• Experience with test-driven development
• Ability to document requirements and specifications

Τοποθεσία: 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.

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 Group Marketing Senior Manager for our offices in Limassol, Cyprus. 

Καθήκοντα:

The Responsibilities include but are not limited to:
• Be responsible for executing global marketing initiatives to drive business growth including innovation in the way we conduct business, customer/patient connections, path to purchase strategies, insight development & deployment, brand positioning, pricing strategy, expansion strategy, retail facing category vision and strategy for the Company’s OTC/ Consumer Healthcare brands.
• Collaborate with Area Sales Leads around the globe to develop multiple marketing programmes. 
• Develop commercial business development programs for all regions. Create and foster strong strategic partnerships with Sales and other business leaders.
• Coordinate and proactively facilitate the identification of new business opportunities, strategic and operational analysis of opportunities, including leading the vetting and validation of ideas and opportunities. 
• To act as single point of contact for our global regions helping to maximise their potential growth.
• Adapt a central multi-channel communications programme ensuring high cultural resonance for all regions and the probable addition of alternative copy for any specific local challenges. 
• Partner with R&D, Regulatory, Sales, Regional Marketing, Finance and key customers in planning, coordinating and sequencing product launches and customer targeting. 
• Support business financial objectives and ensure applicable company compliance with all relevant country and regional requirements, company regulations, policies and procedures.

Προσόντα:

• Bachelor’s degree is required with science expertise as preferred.  Master’s Degree in business or marketing will be preferred.  
• 15+ years of marketing or related function experience in the pharmaceutical industry with 5 years in management-level positions with increasing responsibilities. A demonstrated record of accomplishments regarding business development strategies, brand marketing and portfolio management.
• Deep understanding of the pharmaceutical industry across a range of lenses (e.g. Marketing, Sales, Medical Affairs, Market Access, etc.)
• People management experience and high propensity for people development. Experience in leading cross-functional teams will be considered as advantage. 
• Experience in leading business growth in complex global framework.
• Ability to travel.
• Fluency in English language both verbal and writing. 

Τοποθεσία: 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 Group Senior Product Manager for our offices in Limassol, CYPRUS. 

Καθήκοντα:

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

Προσόντα:

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

Τοποθεσία: 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 (GMP).

Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Assurance Specialist (Risk Assessment) in our offices in Limassol, CYPRUS.

Καθήκοντα:

• Coordinate the Risk Management process/ function within the company 
• Perform risk assessments
• 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
• Regular follow up on the progress of the mitigation plans and update the status
• Support risk management process for projects in co-ordination with project manager / leader.

Προσόντα:

• Bachelor's degree in a science discipline
• Minimum of 3+ years experience in the Pharmaceutical Industry 
• Knowledge and understanding of Quality Assurance, GxP requirements and Quality Management Systems
• Hands on risk management experience within pharmaceuticals will be considered as advantage 
• Excellent command of the English language, both written and oral
• Strong computer literacy skills
• Ability to work in a team environment and prioritize work in a dynamic and fast moving environment.

Τοποθεσία: 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.   

Καθήκοντα:

• Coordinate, supervise and control production processes to ensure that products are produced according to the appropriate procedures in order to obtain the required quality.
• Monitor the compliance of the department with the requirements of Good Manufacturing Practice (GMP).
• Carry out the production plan according to the production schedule.
• 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). 

Προσόντα:

• 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

Τοποθεσία: 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.   

Καθήκοντα:

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.

Προσόντα:

• 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.

Τοποθεσία: 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 

Προσόντα:

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

Τοποθεσία: 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.

Καθήκοντα:

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

Προσόντα:

• 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

Τοποθεσία: Λεμεσός, ΚΥΠΡΟΣ

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)

Καθήκοντα:

• 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 

Προσόντα:

• 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

Τοποθεσία: Λεμεσός, ΚΥΠΡΟΣ

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. 

Καθήκοντα:

• 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 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 τα υπόλοιπα τμήματα για τη διασφάλιση της εύρυθμής λειτουργίας του τμήματος.  

Προσόντα:

• Κάτοχος πτυχίου Μηχανολόγου Μηχανικού, Μηχανικού Παραγωγής, Ηλεκτρολόγου Μηχανικού, Χημικού Μηχανικού ή άλλες συναφή σπουδές.
• Απαραίτητη εργασιακή εμπειρία τουλάχιστο ενός χρόνου   
• Προϋπηρεσία στη Βιομηχανία ή σε Επιστασία προσωπικού θα θεωρηθεί επιπρόσθετο προσόν. 
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.

Τοποθεσία: 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 Technology Transfer Manager for our offices in Limassol, CYPRUS.  

Καθήκοντα:

• 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.

Προσόντα:

• 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.

Τοποθεσία: 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.  

Καθήκοντα:

• 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.

Προσόντα:

• 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.

Τοποθεσία: 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 Formulation Associate for our offices in Limassol, CYPRUS.

Καθήκοντα:

• 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

Προσόντα:

• 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

Τοποθεσία: 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.