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To be an integral part of an antibody development team with a focus on performance and improve customer outcomes through validation of cell culture workflows, reagents, and consumables.

Bachelors degree in Chemical, Biological, Medical Laboratory Technology, Pharmaceutical Sciences in relevant fields from a UGC, AICTE recognized University, Institute ; One year experience in Chemical and or Bio-Chemical analysis preferably in Drug testing.

SCIENCES OR PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 5 YEARS EXPERIENCES IN PARENTERAL MANUFACTURING VIAL, AMPOULES, BOTTLES OF GLASS OR PLASTIC THROUGH, LVP/SVP WITH BFS TECHNOLOGY. CANDIDATE WORKED IN PRODUCTION COMPLIANCES, REMEDIATION AND HAVING EXPERIENCES OF MANAGING QUALITY SYSTEM DOCUMENT

Maintain Clarivate database with up-to-date and accurate Clinical trials information from a range of information sources. Accountable for the delivery of weekly targets.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma. Candidate must have hands on experience in Sterile, Parenteral, Aseptic, Filling, Sealing, Filtration, Production QMS, Batch Manufacturing.

To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods.

Should be able to develop analytical methods and perform analysis on UV, Dissolution, HPLC and ICP-OES instruments. Dissolution development, Comparative dissolution profile and multimedia dissolution study.

B.Pharm/M.Pharm/B.Sc/M.Sc; Production and Packaging, Planning, Monitoring and Reporting production activities. Purchase and procurement planning, monitoring and reporting purchase activities

Candidate should have strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements. Monitoring critical process parameters during manufacturing. Candidate should have sound knowledge of QMS - Incidents, Change control, Deviations etc. Should be able to handle the team of 8-10 persons