AVENZA-INTERVIEW on 02 March 2024
PHARMA REQUIREMENT WALK IN… A
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
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.
Qualification: M. Sc / B. Pharm/M. Pharm Relevant Experience: 3-6 years in Pharmaceutical Formulation Quality Control Lab OR Analytical Development/Method Validation Lab.
AVENZA PHARMACEUTICALS PVT LTD Plant: 111/1, Jarod-Samlaya Road, Tal. Savli, Dist. Vadodara Landmark: next to Meena Circuit
WALK-IN – INTERVIEW Date: 02 March 2024 (Saturday) TIME: 10.00 am to 17.00 pm Contact: 9773433264
