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Zydus Biologics Urgent Openings for Quality Control /Quality Assurance-Apply Now

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Zydus Biologics Urgent Openings for Quality Control /Quality Assurance Department-Apply Now

Zydus Biologics Urgent Openings

About Company:

Zydus Biologics (also known as Zydus Cadila) is an Indian multinational pharmaceutical company headquartered in Ahmedabad, Gujarat, India primarily engaged in the manufacture of generic drugs. It ranked 100th in the Fortune India 500 list in 2020. Cadila was founded in 1952 by Ramanbhai Patel (19252001), formerly a lecturer in the L.M. College of Pharmacy, and his business partner Indravadan Modi. It evolved over the next four decades into an established pharmaceutical company.

Inviting candidates for Executive/Senior Executive posts in Quality Control/ Quality Assurance for Zydus Biologics (Zydus Biotech Park) at Ahmedabad

DepartmentQuality Control
DesignationExecutive/Senior Executive
QualificationM.Sc.-Biotech/Biochemistry
Experience03 to 06 years
Applying LinkApply Now

QC Chemical: Candidates should have experience in the analysis of protein analysis/ instrumentation, molecular biology, bioassay, and lab activity-related documents. They would be responsible for reviewing all the documents, test reports, calibration reports records, logbooks, and formats in relation to the activity of protein analysis/ Instrumentation, molecular biology, bioassay, and filling. They would also be responsible for carrying out investigations of incidents, deviations, and OOS generated during laboratory analysis.

QC Microbiologist: Should be responsible for environmental monitoring (air sampling, settle plate, surface monitoring, and personnel monitoring)/water testing/bioassay/BET test/MLT/sterility testing, etc.

Department: Quality Assurance
IPQA candidates should have experience in QA oversight (IPQA) related activities
for drug substance manufacturing along with handling process validations, batch release activities, cleaning validations, process investigation, and OOS/OOT. the investigation, change control, deviation, CAPA, and QMS activities.

For all the above positions, candidates have been exposed to the regulatory requirements of
documentation and cGMP/GLP is essential.

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