Job Overview
-
Date PostedDecember 17, 2023
-
Location (State / UT)
-
Expiration dateMarch 19, 2026
-
Experience10 Years, 16 Years
-
GenderAny
-
Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities:
- Lead and guide site investigation teams to investigate the reported OOS, OOT, Deviations and Market complaints by working closely with site CFT and operating personnel, to find out the appropriate RCA and CAPA.
- Review and improve quality of investigations of other investigation members in terms of technical report writing skills as per format.
- Support to site during regulatory inspection or audits / Inspections conducted by local regulatory bodies/vendors / third parties, for related investigation.
- Practical knowledge and troubleshooting skills of various analytical instruments like HPLC, GC, KF, XRD, PSD by Malvern, UV etc.
- A person should have exposure of analysis of solid oral dosage forms or Ophthalmic dosage forms or MDI-DPI & Derma dosage forms.
- Well-versed in cGMP, GxP practices.
Desired Candidate Profile:
Position – Manager – QA
Experience – 10 to 15 Years
Qualification – B. Pharma / M. Pharma, MS/M.Sc