Anthem BioSciences Quality Control Analytical ( Biologicals) Openings
Anthem BioSciences Quality Control Analytical ( Biologicals) Openings 2022
Vacancy Information described below interest & Eligible candidates apply Now
About the Company :
Anthem Biosciences is one of India’s leading vertically integrated biopharmaceutical research and manufacturing organizations, offering end-to-end services and a wide range of chemical and biological therapeutic products. We cater to biopharmaceutical, healthcare, and academic institutions across the globe. Our 100+ acre campus spread over 5 sites and 20 blocks, houses state-of-the-art R&D centers and CGMP compliant manufacturing units. Our manufacturing units have been successfully audited and approved by USFDA, DCGI, and other regulatory agencies,
At Anthem, we are increasing our focus on the development, manufacturing, and commercialization of a wide range of biological products expressed from both microbial and mammalian cells. We have carved our niche in the CDMO space working with global clients for both biosimilars and NBES. We are expanding our product portfolio, manufacturing infrastructure and market reach in this highly specialized therapeutic segment. We are looking for biopharma professionals who would like to be part of this exciting journey.
Department: Quality Control – Analytical (Biologicals)
Qualification: MSc Biotechnology /Biochemistry
Experience: 2 to 5 years
Requirement:
Must have experience in Western blott, ELISA, HCP and HCDNA, SDS PAGE electrophoresis, potency assay techniques
Highly proficient in the use of key analytical equipment (ELISA, Gel Doc, HPLC, CZE, UPLC and UV spectrophotometer) and the testing of finished products
Preparing Quality reports, including analytical reports (finished products). Certificates of Analysis (COA) (for finished products) and stability reports.
Creating and executing method transfer and method validation test protocols for finished products and generating the appropriate analytical methods.
Stability testing of products for new formulations and ongoing stability trials
Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specifications
Writing/reviewing Standard Operating Procedures (SOPs)
Calibrating analytical equipment, as and when required.
All laboratory work undertaken is performed in accordance with CGMP quality system.
Prefer candidates with prior QC-analytical experience who can work round the clock shift system
LAST DAY FOR SUBMISSION: 27TH MARCH 2022
SEND YOUR CV’S TO [email protected]
