B.Sc

Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc. QC investigation and QMS

Experience in handling QC instruments like HPLC, LCMS, GC, UV - spectrophotometer, dissolution apparatus, KF, IPC-OES, IR spectrophotometer

Bachelor of Pharmacy. Independently drafting, negotiating, and finalizing new agreements, and amendments to existing agreements, as per Pharmacovigilance Agreement, PVA standard operating procedures.

Sciences or Pharmacy Graduates B.Sc./M.Sc./B. Pharm./M.Pharm. with 0 to 2 years Experiences in parenteral manufacturing QMS / IPQA. Candidate worked in compliances / remediation / and having experiences of managing quality system document CCN / CAPA / investigation etc.

Diploma, B.Pharma, Bsc and Msc applicants can apply. Experience in IPQA, QMS , LMS. Candidate having experience to handle BFS/FFS machine and autoclave operations with troubleshooting. Candidate having experience with rommelag/weiler machine preventive maintenance.

Graduation mandatory. Science/Pharma Graduate preferred . Should have relevant Team Handling and Pharma experience

Quality Assurance, QA Fill Finish, QA Biosimilars, QA Insulin Fill Finish, Biosimilars, Insulin, IPQA, QMS, Audit and Compliance, AQA. Aseptic Manufacturing, Vial Washing, Filling, PFS & Sealing, QM

B. Pharmacy/ M Pharmacy / Msc / Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / QMS activities; QUALITY ASSURANCE Validation & Qualification, IPQA

B.SC., M.Sc., B.Pharm, M.Pharm, B.Tech, M.Tech any Science; Responsible for check that Pharmaceutical products & Perform the analysis as per requirement of test request for R&D department.