Analytical Development Bioassay Senior Scientist
Demo S.A.Athens, Attica, Greece
Posted October 14, 2025
Full Time
About the Company
DEMO is a dynamic Greek industrial and commercial organization, specializing in the development, production and supply of pharmaceutical products. The company is the largest supplier of injectables for public hospitals in Greece, exports 80% of its annual production and is recognized as one of the official suppliers of the United Nations, UNICEF, the World Health Organization (WHO), Doctors Without Borders and the International Committee of the Red Cross. With over 3,300 circulation licenses in 86 countries worldwide, the largest factory in SE Europe and over 1,400 employees, DEMO paves the way for pharmaceutical self-sufficiency for Greece and Europe. Today, DEMO implements investments of €356 million, strengthening production and R&D, while entering the development and production of active ingredients and Biotechnology. At the same time, the company is committed to ensuring equality, diversity and inclusion in the working environment and has adopted -within this context- the Diversity Charter for Greece. DEMO moves "Always Forward" driven by its corporate philosophy of providing quality and reliable pharmaceutical products, for everyone. Learn more at www.demo.gr
Job Description
DEMO SA, a leading pharmaceutical manufacturer, is seeking a Bioassay Senior Scientist to join their team in Athens, Greece. This role focuses on developing and qualifying methods for characterization and quantification of biosimilar products, designing experimental protocols, and providing scientific insights to guide decision-making. Collaboration with cross-functional teams and adhering to regulatory guidelines are key aspects of the position.
Requirements
- MSc in Biology, Biotechnology, Biochemistry or related field
- PhD in a field related to Biology, Biotechnology, Biochemistry, Molecular Biology
- More than 4 years of industry experience in monoclonal antibodies and biosimilars
- Strong expertise in protein analysis techniques (ELISA, Molecular biology, SPR, Q-PCR)
- Familiarity with regulatory requirements for biopharmaceutical characterization
- Excellent communication and problem-solving skills
- Strong software skills (Excel, Data visualisation, statistics)
- Experience in quality system – GMP, GLP or Good Development Practices
Benefits
- Competitive remuneration
- Continuous learning and development opportunities
- Friendly and challenging working environment