As a drug product project leader you will play a key role in the development of formulations and processes for parenteral dosage forms of Biologics (e.g. monoclonal antibodies, therapeutic proteins, conjugates and other new modalities) for clinical or commercial use. Your responsibilities include: - Strategic lead of Drug Product Development within Biologics projects and be accountable for agreed upon deliverables to the CMC team - Author or review regulatory CMC documents and communicate with health authorities, if required - Oversee and contribute to design, planning, performance and interpretation of scientific experiments for the pharmaceutical development of stable liquid and lyophilisate formulations, robust manufacturing processes of syringes, cartridges and vials
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company.
If you are interested then kindly send your resume to: firstname.lastname@example.org
- Minimum of 2-5 years of successful experience in biotech / pharma industry with emphasis on biologics drug product formulation and process development, manufacturing, scale-up, and technology transfer - Experience in protein analytics, lyophilization, primary packaging development for biologics as well as regulatory submissions is an advantage - Excellent scientific leadership skills, interdisciplinary thinking and proven ability to work in cross-functional, international teams - Strong presentation skills and scientific/technical writing skills
Ph.D. in Chemical Engineering, Biochemical Engineering, Pharmaceutical Technology, or equivalent
English : Very good