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 attract a Research Scientist to join our Analytical Development APIs team at Pharmathen’s Pallini premises.

As a Research Scientist you will provide high quality analytical method development and validation in a GMP environment. You will also support new product development through analysis of innovator samples and R&D formulations.

More particularly:

What you’ll do:

Participate in the development and validation of analytical methods and improvement of existing ones to support all stages of drug development from drug substance characterization through formulations and process development Prepare and review analytical data, technical reports and analytical methods in support of and for inclusion in the regulatory submissions Compile, maintain, review and interpret analytical and statistical data; assist with generating high quality technical documents required for method validation Prepare high quality technical documents required for analytical purpose Maintain and follow all laboratory systems, GMPS Adhere to safety and housekeeping requirements Manage deliverables and ensure that necessary supplies such as: standards, reagents, columns, impurities are available on time for projects Prepare SOPs, as required