Τοποθεσία Αχαρνές πριν 2 μέρες Ημ. ανάρτησης πριν 2 μέρες Με κάποια εμπειρία Επίπεδο εμπειρίας Με κάποια εμπειρία Πλήρης απασχόληση Τύπος απασχόλησης Πλήρης απασχόληση Φαρμακευτικά / Υγεία Κατηγορία θέσης Φαρμακευτικά / Υγεία
KLEVA Pharmaceuticals S.A. is a privately owned pharmaceutical company that has been in operation in Greece since 1974. Kleva develops and manufactures generic products and focus on Pharmaceuticals (Rx & OTC).

KLEVA is a fully integrated company with R&D, RA, Production, QC, QA, Marketing and Sales departments.

Our factory in Athens, Greece, is equipped with the latest technology machinery and has the manufacturing potential for a wide range of pharmaceutical forms.

Our mission is to offer a flexible, fully scalable, qualitative, and cost-effective product development in a wide range of dosage forms. We register and export our products to a number of regulated and non-regulated markets around the world.

To realize our ambitious goals, KLEVA needs people who are innovators, believe in the values of respect and cooperation and are ready to commit to a company that wants to penetrate new markets, leverage international business development opportunities, and enter contract manufacturing deals.

How you will support our mission:
We are looking for a C hemistry, M anufacturing & C ontrols (CMS) Officer to join the team at our Product Development Dpt. The successful candidate will take on a challenging and demanding role with primary objective the compilation and review of the Common Technical Document (CTD) of pharmaceutical products.

Main responsibilities

Coordination, compilation and review of CTD of pharmaceutical products

Support during dossier assessment by competent authorities following strict timelines

Communication and close collaboration with laboratory and manufacturing site of the company in order to collect the required data for compilation of the CTD dossier

Support the transfer of the procedures to production

Keep updated on regulations and guidelines published by competent authorities

Qualifications and experience

Bachelor’s degree in Sciences (preferably Pharmacy or Chemistry)

Fluency in English both written and oral

Previous professional experience of at least 2 years in a pharmaceutical company in the field of dossier compilation

Excellent computer literacy (MS Office)

Be multitasking

Cope with deadlines

Excellent work in a team

Benefits

Work in a friendly and challenging environment

Competitive salary

Private insurance

Personal development opportunities