AVENZA PHARMACEUTICALS PVT. LTD is WHO – GMP Approved / Regulatory Complying Manufacturing Unit of OSD facility having vacancies in QC & Analytical Development Lab, (Subject Matter Experts in following areas), at AVENZA PHARMACEUTICALS PVT. LTD. – VADODARA
Job Description:
Quality Control Lab
- Hands on experience on HPLC/GC/ Dissolution/PH/Balance & other QC instruments.
- Lab Documentation Should have experience in Laboratory Data Review, Good at documentation and Audit trail Handling.
- Must have analysis exposure of raw materials and oral solid dosage analysis on HPLC and GC.
- Should have skill of HPLC/GC trouble shooting and electronic data review.
- GLP-Calibration of HPLC/ Dissolution Test Apparatus/PH Meter/Balance & other QC instruments.
- Exposure to regulatory requirement.
- Should have knowledge of compendia procedure and good documentation skill
Analytical Development Lab / Method Validation:
- Method Validation-Analytical Method Validation and verification
- Must have thorough knowledge of regulatory requirement for method validation.
- Should have exposure in method validation analysis by HPLC/GC.
- Should have documentation skill of protocol/report preparation.
- Handling of investigation and compliance of GMP.
Eligibility:
- Qualification: M.Sc / B.Pharm/M.Pharm
- Relevant Experience: 3 – 6 years in Pharmaceutical Formulation Quality Control Lab OR Analytical Development/ Method Validation Lab.
WALK-IN – INTERVIEW DETAILS:
- Date: 02 March 2024 (Saturday)
- TIME: 10.00 am to 17.00 pm
- Venue: AVENZA PHARMACEUTICALS PVT LTD Plant: 111/1, Jarod-Samlaya Road, Tal. Savli, Dist. Vadodara Landmark: next to Meena Circuit
- Contact: 9773433264
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