Cadila Healthcare Limited ( Zydus VTEC Limited ) Walk-in Interview 2021 M. Tech/ B. Tech with Biotechnology, M.Sc. (Biotechnology) for Manufacturing /Quality Control/Quality Assurance At Ahmedabad. Cadila Healthcare Limited ( Zydus VTEC Limited ) Notification full details below.Interaested and eligible candidates can attend interview on scheduled time and venue.
- Vacancy details:
- Post Name: Manufacturing /Quality Control/Quality Assurance
- Qualification: M. Tech/ B. Tech with Biotechnology, M.Sc. (Biotechnology)
- Experience:02 to 7 years
Job Description: Cadila Healthcare Limited ( Zydus VTEC Limited ) Hiring For Manufacturing /Quality Control/Quality Assurance !
- Important Details :
- Location: Ahmedabad
- Contact – Arvind Kumar Singh (08016095113)
- Post of date:24/12/2021
- Selection Process: The selection will be on the basis of Interview.
- Walk-in Interview Manufacturing /Quality Control/Quality Assurance , Cadila Healthcare Limited ( Zydus VTEC Limited )
Interview Dates:26th December, 8.30 AM – 6.00 PM
Venue:-Hotel Radisson, Hi Tech City, Ganchibowli, Hyderabad, Telangana-500032
Manufacturing (Upstream Process):
With 2-8 years of hands on experience of handling equipment such as fermentation Process, Automated fermenters, continuous centrifuges, filtration skids, Automated CIP & SIP units, Knowledge to perform aseptic handling, knowledge of GMP documentation. Must be familiar with cGMP requirements.
Manufacturing (Downstream Process):
Experience in formulation & filling. Should be able to operate chromatography column ( large volume ), Automated TFF Systems, DS filtration activities inside B&C grade. Knowledge of media/buffer preparation & reagents as per defined system.
Good Knowledge of QMS – GMP documentation.
Must be familiar with cGMP requirements.
Quality Control – Protein analytics/Bio assay/Microbiology/Physico chemical/RM-PM :
With 2-8 years of hands on experience of handling equipment & tests such as HPLC/UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA, Bioassay, microbial identification, microbiological testing of material/products, sterility testing, BET, environmental monitoring of cleanroom, RM/PM, handling stability studies, Animal Handling & Testing (DPT Vaccines), Cell Culture Handling & Testing. Must be familiar with cGMP requirements.
With 2-8 years of hands on experience of IPQA activities, Line clearance procedure and practices, Aseptic area practices, cell banking/seed lot system procedures, reviewing of batch manufacturing records, handling of qualification/validation activity, change control, deviation, investigation, CAPA, QMS, self-inspection, vendor qualification activities. Awareness of cell banking/seed lot system procedures, Must be familiar with cGMP requirements and working experience in sterile injectable manufacturing facility/vaccine/biologicals will be preferred.
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