Pharmathen is one of the leading complex drug delivery and formulation developers and is among the top 50 pharmaceutical research companies in Europe. Driven by innovation, the company specializes in one of the most modern and technologically innovative sectors, developing Long Acting Injectables (LAI), Sustained Release formulations and Preservative Free Ophthalmics.

Pharmathen’s portfolio consists of over 100 products, produced at its facility in Sapes, Rodopi, approved by the US Food and Drug Administration (FDA), and at its modernized production unit in Pallini, Attica.

Pharmathen is one of the largest private investors in research and development in Greece, with steady investments of €35 million annually in the R&D sector and employs over 1,350 people from over 24 different nationalities. The company's enduring success is attributed to the passion for creativity, the ethics, and dedication of its people, who share 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 RAW Materials Junior Reviewer at our Sapes premises.

As a RAW Materials Junior Reviewer you will review and approve manufacturing, filling and Packaging records of RAW materials and finished products.

More particularly:

What you will do:

Follow Company's Quality Policy and complies with current operational standards and legislative requirements 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 Follow the rules of hygiene and control of health status as defined in the relevant Policies and Standard Operating Procedures Maintain Quality Systems covering: document control, specifications, SOP’s,  and regulatory documents Create, maintain, and update COA/COC and Specifications Generate and maintain new Batch/Fill Specs instructions for pre-weigh, blending, filling, and packaging activities Maintain Change Control, ERP system and Batch/Fill Specs database Review Batch/Fill Cards for proper compliance with established specifications Conduct Annual Drug Reviews and Device History Reviews