M.Pharm

Responsible for In-process production related activities in DP manufacturing, filling, and packing sections. Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records.

Any M.Pharmacy / MSc (Full time) with 6 to 10 Years (or) B.Pharmacy with 8 to 12 Years of relevant Experience in Manufacturing (Upstream/Downstream) injectables with Strong people management

should possess M.S. (Pharm.) or M. Pharm. in Medicinal Chemistry/Biotechnology, M.Sc. in Chemistry/Life Sciences, PG degree in other relevant branches of Chemical Sciences at NIPER

Master of Pharmacy, Bachelor of Pharmacy, Diploma in Pharmacy. State Pharmacy Council Registration

Post Graduation in Pharmacology, Biotechnology, Bio-informatics, Molecular Biology. Minimum 01 year experience in Research after Post Graduation.

Postgraduate Degree in Science (M.Pharm, Life Science, Biotech, Zoology, Botany) with Mandatory Post Graduate Diploma in Clinical Research and one-year clinical research experience. OR MSc in Clinical Research.

Routine microbiological testing and environmental monitoring to ensure compliance with regulatory standards and GMP guidelines.

Post Graduates in Life Sciences / Pharmacy/Statistics/Social works/ Sociology/BAMS,BSMS and MD in AYUSH with at least 55% marks with one year of post qualification experience in the related field.

Review documents required for regulatory submissions across global markets, including product development reports and scientific justifications for responding to regulatory queries.