Zydus Biologics Limited Walk In Interview 2023 . Zydus Biologics Limited Notification full details below.Zydus Biologics Limited (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.
Vacancy details:
- Post Name: Executive/ Senior Executive post in Quality Control / Quality Assurance
- Qualification: M.Sc. – Biotech/ M.Sc. Micro/ M.sc Biochemistry background.
- Experienced: 2-6 years
Job Description: Greetings from Zydus Biologics Limited !!!!
Important Details :
- Location: Ahmedabad, Gujarat, India
- Salary: Not Disclosed by Recruiter
- Post of date:15/08/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Quality Control
QC Chemical: Candidates should have experience in 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 investigation of incident, deviation 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 /bio assay /BET test /MLT/sterility testing etc.
Quality Assurance
IPQA – Candidates should have experience in QA oversight (IPQA) related activities for drug substance manufacturing along with handling of process validations, batch release activities, cleaning validations, process investigation, OOS/OOT investigation, change control, deviation, CAPA and QMS activities.
QMS: Experience in QMS related activities like failure investigation, quality events handling and investigations, change control, market complaint, conducting self-inspection, APQR, OOS/OOT trending etc.
QA Analytical: Should have experience in reviewing of analytical batch docket/reports, stability protocols and data sheets, laboratory investigation, reviewing and involvement in investigation of OOS, OOT, OOC results, handling of incidents, deviations, Change Controls in the laboratory along with reviewing of all types of calibration / qualification documents and reviewing / oversight implementation of all lab standard operating procedures.
Documentation cell: Experience in handling and controlling of various GMP documents (issuance / control / retrieval / archival). Candidates should be responsible for retaining all master/executed documents in document storage room with adequate indexing and keeping ready all the documents for the regulatory audit(s).
For all above positions, candidates having exposure to regulatory requirement of documentation and cGMP/GLP is essential.
