Company Overview: Zydus Lifesciences, a pioneering global lifescience company under the Zydus Group, is dedicated to enhancing well-being by providing high-quality healthcare solutions. With over 23,000 employees worldwide, Zydus focuses on innovation in the discovery, development, manufacturing, and marketing of diverse healthcare therapies.
Walk-In Interview Details:
- Date: 7th July 2024 (Sunday)
- Time: 9:00 AM to 5:00 PM
- Venue: Greenpark Hotels, Begumpet Rd, Leelanagar, Hyderabad, Telangana 500016
Open Positions:
- Quality Control (QC)
- Quality Assurance (QA)
Job Role Overview
| Role | Experience | Qualification | Preferred Experience |
|---|---|---|---|
| Executive / Sr. Executive / Assistant Manager / Deputy Manager – Quality Control | 4-12 Years | M.Sc./B. Tech/ M. Tech in Biotechnology | Virology/Bacterial QC |
| Sr. Executive / Assistant Manager / Deputy Manager – Quality Assurance | 8-12 Years | M.Sc/B.Tech/ M.Tech in Biotechnology | Biotech/Vaccine QA |
| RM/PM | 4-5 Years | M.Sc Chemistry | Raw and Packing material analysis in QC |
Job Descriptions
Virology QC
- Techniques Required: Cell culture based assays, Virus titration, ELISA, RT-PCR, biochemical assays
- Responsibilities: Review and execute analytical plans for Viral vaccine testing, analysis of bacterial or recombinant vaccine testing
- Instruments Knowledge: pH meter, Analytical balance, Karl Fischer, Real-time PCR, ELISA
- Additional Knowledge: Calibration and qualification of equipment and instruments
Bacterial QC
- Techniques Required: Bio-chemical assays, immuno-chemical assays, HPLC based assays
- Preferred Experience: Analysis of Polysaccharide vaccines/ Bacterial vaccines
- Instruments Knowledge: UV spectrophotometer, ELISA reader, HPLC, UFLC, Kjeldahl, IC-chromatography
- Additional Responsibilities: Handling QMS elements like OOS, OOT, change control, and deviation; compliance with GMP/GLP
QMS
- Responsibilities: Initiate Change Control, Incident, Deviation; conduct investigations for OOS results/deviation/OOT results/product recall/market complaints/stability failures
- Additional Duties: Execution of Computer system validation (CSV), online verification of User privileges matrix, IT related Documents for compliance improvement
Quality Assurance (QA)
- Manufacturing (IPQA)
- Ensure shop floor compliance to cGMP and GDP
- Oversee document destruction process
- Ensure compliance of personnel, process, and practice with cGMP requirements
- Sterility Assurance
- Follow procedures at critical production stages to maintain sterility
- Evaluate sterility assurance of process, equipment, and personnel
- Monitor aseptic practices during media fill runs
- Deviation and Process Investigation
- Participate in investigation plans, find root causes, and conduct thorough investigations
- Draw conclusions based on trends and similar deviations
- Technology Transfer, Process Validation, Cleaning Validation
- Verify data in Technology Transfer documents
- Prepare and review Process/Cleaning Validation Master Plan
- Complete SAP/LIMS related activities
- Review deviations/incidences, Change Control proposals, and evaluate validation requirements
Note: Bring your resume, educational certificates, and experience letters to the interview.
For further information, contact us at Zydus Lifesciences Contact Information.
