Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted revenues of over Rs. 8600 crores in FY15.
Position : QA, Production, QC
Experience : 4 – 9 years
Location : Ahmedabad
Desired Profile : B.Pharma – Pharmacy | M.Pharma – Pharmacy
Key Responsibilities are mentioned as below:
QUALITY ASSURANCE :
Sr.Executive / Executive : M.Sc./ B.Sc Chemistry with 4 – 8 year , must be familiar with cGMP requirements, Data Integrity, Document Cell, Batch release process, Trending APR shop floor Operation in API / Bulk Drug Manufacturing.
- Data Integrity – Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.
- Document Cell – Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.
- Batch Release – Knowledge of ICH guidelines and should review of BMR;s and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.
- Technology transfer documents – Review and issuance TTD to plant , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.
- Trending and APR – Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, Trial batch reports, validation Protocols and reports and Annual Review reports.
Sr.Executive / Executive : Diploma /B.E / B.TECH (chemical) M.Sc./ B.Sc. (Chemistry) with 4 to 7 years of experience and relevant exposure in API / Bulk Drug Manufacturing. Should also have knowledge of GMP documentation. Must be familiar with cGMP requirements.
QUALITY CONTROL :
Sr.Executive / Executive : M.Sc /B.Sc (Chemistry) with 4 – 8 years of hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.
How to apply :
Interested candidate may Walk-In for Interview along with their CVs and relevant documents at
Date : 12th March 2016 (Saturday)
Time : 09:30 AM to 05:00 PM
Cadila Healthcare Ltd
Plot No 291, GIDC
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