Gujarat

Dossier & document preparation as per CTD, ACTD & country specific guidelines, Review of dossiers, DMF & Technical documents, Answer query raised from regulatory authority.

Handle manufacturing skids, Fedegari autoclaves isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic/ PFS filling and aseptic filtration

Preparation/review of medical and scientific write up. Coordination for serious adverse event reporting and safety update to Regulatory agency

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

Strong analytical skills, problem-solving abilities, and knowledge of bioanalytical tools are essential.

M.Pharm, MS Pharm, MSc or Equivalent with specialization in Biotechnology, Microbiology or Life sciences. GATE/CSIR/UGC NET/GPAT qualified.

M.Sc. in Marine Sciences / Microbiology / Biotechnology / Life Sciences. The candidates have a good technical writing and event management skills. The candidates will have to work in field also.

Inviting applications from highly qualified and dynamic candidates for the QA, QC, Micro QC, Production, ADL positions at our API Manufacturing Unit

ITI / Any Diploma / B. Pharma / M. Pharma. Calibration / Analysis of RM/FP/PM. Work exp. In QC Instruments