Responsible for maintaining compliance and to ensure GLP in lab
Responsible for preparation of AMV protocols and reports
Responsible to provide request to section head for issuance of AWR and to record analysis related activities
Responsible for execution of Analytical Method Validation/Verification activities in lab
Responsible to carry out AMV activities as per planning
Responsible to participate in investigation generated during AMV activities
Responsible to participate in investigation of OOS/OOT to find out the root cause like verification of force degradation data.
Responsible for preparation calibration and preventive maintenance planner.
Responsible for daily temperature monitoring of QC lab area
Responsible for receipt of Reference Standard, Primary Standard,secondary standards and maintaining the record for the same.
Responsible for preparation of protocol for Cleaning validation related activities and for execution
Responsible to maintain documents as per GLP and GMP system
Responsible to maintain Data Integrity in lab.

Desired Candidate Profile
Candidate Should be from Pharma - injectable formulation background.
Should have knowledge of 21 CFR Part 11.

📌 Sr Officer / Officer Qc Amv Profile Pithampur
🏢 GUFIC Group
📍 Pithampur