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
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.
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.
Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility