- To coordinate with all dept for execution of PV activities & to inform Sub-department Manager about any deviation from planning.
- To review process validation, qualification planner & send it to Sub-department Manager for further review & information.
- To conduct Material issuance for validations activities.
- To ensure Sample withdrawal during process validation & keep Sub-department Manager updated about any deviation.
- To record observations in observation sheets for process validation & sign the same.
- To coordinate among various departments for process validation, qualification activities & keep Sub-department Manager updated.
- To execute validation, qualification activities & inform Sub-department Manager about deviation from planning, if any.
- To conduct new equipment qualification & validation & get reviewed by Sub-department Manager about the same.
Industry: Pharma / Biotech / Clinical Research
Functional Area: Other
Equipment Qualification, Process Validation, Deviation, QA
UG -B.Sc – Any Specialization, Chemistry, B.Tech/B.E. – Any Specialization, Electronics/Telecommunication, Instrumentation, B.Pharma – Pharmacy
PG – MS/M.Sc(Science) – Any Specialization, Chemistry, M.Pharma – Pharmacy