December 2024

Knowledge of QC instruments & handling of trouble shooting of critical Instruments. Defining departmental employee roles, responsibilities and authorities. To monitor upkeep and compliance of laboratory in regulatory view.

Responsible for supporting preparation of high quality technical documents and reports Responsible for strict adherence to quality standards and regulatory guidelines. Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance. Performs other related duties as required.

Applicants must have M.Pharma, M.B.B.S. with post graduate degree or diploma in Medicine from a recognized university, institution.MBA, P.G.D.M. as additional qualification shall be preferred. Consultant Drug Procurement

Candidates should have experience in Formulations regulated manufacturing company such as USFDA and MHRA, EU. Exposure to regulatory audits like USFDA, MHRA, EU is mandatory

Good knowledge on the scale-up factors from RD to EB scale pharmacokinetics of drugs, proficiency in BE studies is required. Experience in responding regulatory Queries for all markets

M.V.Sc, M.Pharma, M.Sc. Biotechnology, Biochemistry, Zoology, Microbiology with Two years experience for PAT-II. Work experience in the area of Laboratory Animal

M.Sc in any branch of Life Science with at least two years of research experience in Cancer Biology. Masters in Natural or Pharmaceutical Sciences OR Bachelor degree in Engineering or Technology from a recognized University or equivalent.

First class Post Graduate in Pharmacology, Biotechnology, Life Sciences and should be selected through a process described in anyone of the following National Eligibility Test CSIR-UGC NET including lectureship Assistant Professorship and GATE.

Graduate in Life Science or B.Pharma and Diploma in Clinical Research with 02 years relevant experience in Clinical Research is mandatory.