Founded in 1969, Pharmathen has grown to become one of the largest, vertically integrated developers of complex drug delivery technologies and is among the top 50 pharmaceutical research companies in Europe.

The company has one of the most extensive and advanced pipelines of long acting injectables (LAI), sustained release and ophthalmic formulations.

Pharmathen’s highly diversified portfolio consists of over 90 commercialized products, which are produced in its US FDA and EU-approved manufacturing facilities in Greece, serving 250 customers and accessed by patients in more than 90 countries worldwide.

Pharmathen proudly employs more than 1,600 people from over 28 different nationalities, with 54% of its total workforce and 66% of its Research Operations Team being female. The company’s enduring success is attributed to a passion for creativity, strong ethics, and the dedication of its people, who share a commitment to the company's vision of making a difference in people’s lives.

Due to continuous growth and expansion, Pharmathen offers a great opportunity for career development and is seeking to recruit a Quality Assurance Junior Officer - Fixed-Term Contract (One Year) to join our Quality Assurance team at our Sapes, Rodopi premises.

As a Quality Assurance Junior Officer, the ideal candidate will be responsible for ensuring compliance with GMP requirements and ISO standards.

More particularly:

Work in accordance with the requirements of the written Policies, Standard Operating Procedures, Technical Directives and Protocols of the company's Quality System, that are related to the duties of the described position Support the Corporate QA, API Industrial operations & follow-up for pending items etc to related activities of report compilation & completion Take part in preparation and authorship of the Quality Management  department’s SOPs,TDRs and other controlled documents of the Quality System of the company Support Regulatory Submission of Dossier Update the master list of all documents concerning Quality System Perform training sessions on new or revised SOPs Maintain file of Quality Agreements and Protocols by subcontracted companies and maintain records on this Participate in all special occasions in regards to the Corporate Quality Management needs and authorizations Participate in media-fill simulation process in aseptic manufacturing area Follow Quality system SOPs in day to day activity