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 Pharmaceuticals offers a great opportunity for career development and is seeking to recruit a Final Products Reviewer to join our Quality Control team at Sapes, Northern Greece premises.

The Final Products Reviewer, reviews Quality Control related documents in order to ensure proper compliance with established Quality Specifications.

More particularly:

What you’ll do:

Maintain Quality Systems covering document control, specifications, SOP’s, and regulatory documents Review Batch records of raw materials, excipients, packaging materials (LAI only), stability studies documentation (LAI only) and finished products for proper compliance with established specifications Create, maintain, and update COA/COC and Specifications Support in activities as Change Control, and ERP system functions Liaise with Quality Assurance and Production department for information exchange so as to support in release procedures.