Bachelor or Master degree in Pharmacy with a specialization in Pharmaceutics or Pharmaceutical Technology. Responsible to Organize and Co-ordinate Training Activities, Preparation of documents and Maintenance of training records. Responsible for material code initiation.
B.Pharm, M.Sc, B.Sc, Candidate should have exposure of cGMP, GLP Knowledge and understanding of regulatory requirements are essential. Experience of formulation quality control Tablets/ Topical/Capsule/ Oral solution/ Gel/ Ointment etc exposure of instruments like HPLC/ UPLC / GC/ IR/ UV/ Dissolution apparatus,KF, ICP,- MS/ ICP-OES.
M.Pharm / M.Sc. in life sciences / MBA; Understanding clients requirement and other regulatory submissions Pharma industry for framing commercial proposal, negotiation, and closure of business contracts. Organizing promotional programs & participation in exhibitions for greater brand visibility including fixing meetings around conferences
M.Sc., B.E, B.Tech, M.Tech (Biotech, Chemical, Bioprocess, Microbiology
With 3-10 years of experience Hands on experience in Upstream, Downstream, Mammalian, Fill Finish, Single Use and Microbial Production etc.
The Regional PV Officer contributes to assure patients safety by complying with all PV Quality System Documents, QSDs and local and international regulatory requirements. The main purpose of the position is to ensure that Bayer Pharmacovigilance standards are met
Bachelors degree or above, preferably in a life science or drug development related field. Ensure data quality by conducting data management activities including data validation, data review, etc. following study timelines. Maintain clear reporting on DM activities in alignment with study teams and management needs.
Diploma in Material Management or any Diploma having Material Management as a subject or Diploma in Pharmacy from a recognised University or Institution or equivalent.