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Walk in interview for QA, QC, Production @ Zydus Cadila

By: Pharma Jobs | Views: 6174 | Date: 17-Oct-2015

Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing Infrastructure Is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).

Walk in interview for QA, QC, Production @ Zydus Cadila

Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing Infrastructure Is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).

We have scheduled a walk-in interview for ADL, R&D, Quality Assurance, Quality Control & Production for Cadila Healthcare Ltd., Dabhasa, Vadodara as following.

Post: Supervisor /Officer /Executive / Sr.Executive

Supervisor /Officer /Executive / Sr.Executive

Quality Control (Protein analytics)
MSc. Biotechnology / Biochemistry  with 2-8 years of hands-on experience of handling equipments such as HPLC/ UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA etc. Should also have knowledge of handling stability studies and GMP documentation and must be familiar with cGMP requirements.

Quality Control (Physico chemical)
M.Sc. Chemistry with 2-8 years of hands-on experience of handling equipments such as HPLC, GC, IR, KF auto titrator, coulometer and melting points and in chemical analysis of raw materials, water and packaging material. Must be familiar with cGMP requirements.

Quality Assurance
B. Pharm/M. Pharm/M.Sc ( Biotechnology/ Biochemistry/ Microbiology) with 2-8 years of hands-on experience of IPQA activities,  reviewing batch manufacturing records, handling qualification/ validation activity, change control, deviation, investigation, CAPA, vendor qualification activities. Must be familiar with cGMP requirements.

Quality Reviewer
M.Sc. Biotechnology / Biochemistry / Microbiology with 2-8 years of experience in review of analytical data, change controls, deviations,  validation and qualification reports and having exposure to investigation of out of specification, out of trend and laboratory incidents. Must be familiar with cGMP requirements.

Manufacturing (Downstream Process)
MSc. (Biotechnology/ Biochemistry) / M.Tech/ B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 2-8 years of hands-on experience of handling equipments such as chromatography systems,  ultrafiltration systems, filtration techniques etc. Should also have knowledge of GMP documentation and must be familiar with cGMP requirements.

Manufacturing (Upstream Process)
MSc. (Biotechnology /Biochemistry) / M.Tech/ B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 2-8 years of hands-on experience of handling equipments such as bioreactors, disc stack centrifugation, filtration techniques etc. Should also have knowledge of GMP documentation and must be familiar with cGMP requirements.

Officer to Manager

Quality Assurance (Vaccine)
M.Sc. (Biotech / Microbiology) with 2-10 years of experience in Quality Assurance (QA) of vaccines / sterile injectables. Should also have experience in QA operations / QMS/ validation/ qualification/ documentation/ compliance.

Quality Control (Vaccine)
M.Sc. (Biotech / Microbiology / Chemistry) with 2-10 years of experience in Quality Control (QC) of vaccines / sterile injectables. Should have experience in QC Finished product testing / raw material testing / microbiological testing.

Bacterial Vaccine Production (TOXOIDS)
M.Sc. (Biotech / Microbiology) with 2-10 years of experience in the production of tetanus / diphtheria toxoids in a commercial plant. Should also be able to handle upstream and downstream processing.

Bacterial Vaccine Production (Polysaccharides)
M.Sc. (Biotech / Microbiology) with 2-10 years of experience in the production of polysaccharides in a commercial plant. Should also have experience in the production of typhoid / Hib -TT in a commercial plant and knowledge of conjugation techniques.
Bacterial Vaccine Production (Fill & Finish): M.Sc. (Biotech / Microbiology) / B.Pharma with 2-10 years of experience in the production of vaccines and biologicals in a commercial plant. Should also have experience in formulation and filling of adjuvenated vaccines in a commercial plant and be able to handle ampoules / vials filling line.

Executive / Sr. Executive
Bacterial Vaccine Production (Packing & Dispatch): M.Sc. (Biotech / Microbiology) / B. Pharm with 4-8 years of experience in the production of vaccines and biologicals in a commercial plant. Should also have experience in visual inspection, labeling and packing of vaccines in a commercial plant and be able to handle automated labeling and packing machines. Should have knowledge of cold chain management and dispatch procedures.


Officer to Sr. Executive
Viral Vaccine Production (Downstream Process): MSc. (Biotechnology / Biochemistry)/ M. Tech/B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 2-8 years of hands-on experience of
commercial purification of recombinant proteins. Should also have sound knowledge of downstream operations / buffer preparation / solubilisation / refolding / chromatography and GMP documentation. Must be familiar with cGMP requirements.

Trainee to Officer
Viral Vaccine Production (Upstream Process): MSc. (Biotechnology / Biochemistry) / M. Tech/ B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 1-4 years of hands-on experience in upstream operations / media preparation / sterilisation. Should also have sound knowledge of the biological processes and GMP documentation. Must be familiar with cGMP requirements.

Officer to Sr. Executive
Viral Vaccine Production: MSc. (Biotechnology / Biochemistry)/M. Tech / B.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 2-8 years of hand- on experience in fermentation of E coli and yeast cultures. Should have exposure to process development, media optimisation and scale up and sound knowledge of GMP documentation. Must be familiar with cGMP requirements.

Date: 18th October, 2015 (9 Am to 5 Pm)
Venue: Pune, The Pride Hotel,
5 University Road, Shivajinagar, Pune-411005
Maharashtra. INDIA
Time: 9 am to 5 pm

Interested candidates may also email their resume toHRZRC@zyduscadila.com or send it by courier to the Human Resource Department, Zydus Research Center, Sarkhej Bavla NH 8 A , Moraiya, Taluka Sanand, Ahemdabad 382210 within 7days.

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Comments
PAWAN KUMAR SHARMA  |  18-Oct-2015 11:36:13 IST
I am having exp. Of 2.5 years in ZEE LABORATORIES LTD. PAONTA SAHIB HIMACHAL PRADESH IN SOFT GELATIN AS PRODUCTION CHEMIST.
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