Research Scientist at Pharmathen

Municipality of Metamorfosi, Attica, Greece -

Full Time

Start Date

Immediate

Expiry Date

24 Dec, 25

Salary

0.0

Posted On

25 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Method Development, Method Validation, Drug Development, Formulation Analysis, Data Interpretation, Technical Documentation, Laboratory Systems, GMP Compliance, Safety Compliance, Communication Skills, Computer Literacy, Troubleshooting Skills, Project Management, Team Collaboration

Industry

Pharmaceutical Manufacturing

Description

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 attract a Research Scientist to join our R&D Finished Dosage Forms team at Pharmathen’s Metamorfosi premises. As a Research Scientist the ideal candidate willprovide high quality support in analytical and formulation development in a GLP environment. Supports all stages of a new product development and through preparation and analysis of R&D formulations. More particularly: What you’ll do: Perform the analytical method development & method validation of complex drugs to support all stages of drug development from drug substance characterization to finished product characterization, stability and support. Participate in analysis of formulation /manufacturing process trials. Deliver, evaluates and interprets experimental data Compile, maintain, review and interpret analytical and statistical data. Assist with the generating high quality technical documents required for method validation, stability, formulation and deficiency letters Maintain and follow all laboratory systems, GMPS Follow the rules as defined in the relevant EU and FDA guidelines Adhere to safety and housekeeping requirements Assume other activities and responsibilities as directed The ideal candidate should have: BSc Degree in Chemistry or relevant field /Technical institution degree At least 8 years of practical knowledge gained through experience accompanied by a technical or vocational training At least 2 years of experience in the Pharmaceutical Industry or equivalent experience Job-Specific Skills: Excellent communication in English language (writing & speaking) Computer literacy (Microsoft office). Troubleshooting skills Demonstrated ability to work on multiple projects and meet timelines High team working spirit What you'll gain: Involvement in a high-caliber, team-oriented and dynamic atmosphere Exposure to challenging business issues and practices Great opportunity to leverage and develop your business knowledge and skills Join our team and experience the unique Pharmathen’s culture that gives you the opportunity to innovate, to make decisions, to achieve your own potential and to chart your own career! Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.

Responsibilities

The Research Scientist will provide high-quality support in analytical and formulation development in a GLP environment, supporting all stages of new product development. Responsibilities include performing analytical method development, participating in formulation analysis, and maintaining laboratory systems in compliance with EU and FDA guidelines.