Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies.
M.Sc. in Analytical Chemistry, Applied Chemistry, M. Pharm Pharmaceutical Analysis, Chemistry, Biochemistry, Microbiology, Biotechnology, Botany from a recognized University or equivalent
The ideal candidate should have a proven track record in method development for NCE molecules, a deep understanding of column chemistry used in HPLC, and significant experience with purification techniques. Responsibilities will include troubleshooting and calibration of analytical instruments, managing complex research projects, and ensuring timely, high-quality delivery.
Masters in any area under biology, bioengineering, medical biotechnology, or life sciences disciplines. Individuals with experience in model system re-search or with wet lab experience in cellular or molecular biology, or bioengineering will be preferred. Freshers with fellowships will be preferred.
Should have experience in Line Clearance, BMR Review. Knowledge in Investigations, Risk assessment, deviations, change control and CAPA. Sound Knowledge in QMS.
This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab.