1-2

Perform chemical and physical analysis of raw materials, in-process samples, and finished products. Operate analytical instruments like HPLC, GC, UV Spectrophotometer, FTIR, Dissolution apparatus, etc. Conduct stability studies and routine sampling/testing as per SOPs.

Should have knowledge of country specific dossier preparation. Should have knowledge of country specific dossier preparation

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines

As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

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