AVENZA-INTERVIEW on 02 March 2024

AVENZA-INTERVIEW on 02 March 2024

AVENZA-INTERVIEW on 02 March 2024

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

Job Category: pharma
Job Type: Full Time
Job Location: - Vadodara Gujarat

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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