Zydus Cadila is headquartered in Ahmedabad, India, and ranks 4th in the Indian pharmaceutical industry. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil. Zydus’ global business has a strong presence in the regulated markets of the US, Europe (France and Spain) and in the high profile markets of Latin America and South Africa. It is also present in a big way in 25 other emerging markets worldwide.
Looking for B.Tech Biotechnology / B.E Biotechnology / M.Sc. Biotechnology / M.Sc. Microbiology with 01 to 12 years of hands on experience on CIP/SIP of the equipment, Process vessels, Cold rooms and freezers with an experience of commissioning and qualification for below mentioned openings:
Executive / Senior Executive / Assistant Manager / Dy. Manager
Production – Upstream
Processing Responsible for handling bacterial fermentation process, continuous centrifuge, 1 kl – 5kl fermenters, shaker incubator, continuous centrifuge, LAF procedure
Production – Downstream
Processing Responsible for downstream purification process for recombinant products, handling of equipment such as TFF system, chromatography system, depth filtration procedures.
For all above positions, candidate having exposure to regulatory requirement and cGMP/QMS knowledge is essential.
Interested candidates may send their updated CVs along with current and expected CTC to email@example.com
Quality Assurance department
Looking for M.Sc.(Biotechnology)/M.Sc. (Biochemistry)/M.Sc. (Microbiology)/ B.Pharm / M.Pharm with 1 to 7 years of hands on experience for below mentioned openings:
Officer / Executive / Senior Executive
QA Oversight manufacturing (IPQA) : Code 1
Should be responsible for QA Oversight (IPQA) related activities for Drug substance manufacturing along with handling of process validations, cleaning validations OOS, change control, deviation, investigation, CAPA and QMS activities.
Qualification/Validation : Code 2
Should be responsible for Equipment Qualifications (Fermenter, Bioreactor, Media/buffer preparation Vessels, Autoclave etc.), Utility Qualifications, HVAC, Water System, Protocol preparation and its compilations. Should be responsible for Media fill activities, protocol & BMR preparation/review.
QMS : Code 3
Should be responsible for QMS related activities like Failure investigation, Quality events handling and investigations, change control, market complaint, conducting self-inspection, APQR, OOS/OOT trending etc.
Analytical QA : Code 4
Should be responsible for review of Analytical Reports, Stability Protocols and data sheets, Investigation, Review and disposition of OOS, OOT & OOC results, handling of Incidents, Deviations, and Change Controls in the Laboratory along with review of all method transfer / method validation, types of Qualification documents. Review and approval of all Lab Standard Operating Procedures.
Document control/Documentation cell : Code 5
Should be responsible for handling and control of various GMP documents (Issuance / control / retrieval / archival).
Responsible to retain all master/executed documents in document storage room with adequate indexing and keep ready documents for the regulatory audit(s) For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential.
Interested candidates may send their updated CV along with current and expected CTC to firstname.lastname@example.org
Quality Control Department
Looking for M.Sc.(Biotechnology)/M.Sc. (Microbiology) / B. Pharm / M.Pharm with 1 to 7 years of hands on experience for below mentioned openings:
Officer / Executive / Senior Executive
QC Chemical: Code 1
Should be responsible for Viral vaccine testing, DNA concentration by OD (Optical Density) in multimode reader, DNA form for Supercoiled plasmid content, Residual host cell DNA/ RNA/ Protein (RT PCR / ELISA method) , Knowledge of HPLC, UV Spectrophotometer, Osmometer, Karl-Fischer apparatus
QC RM/PM: Code 2
Should be responsible for physico-chemical testing for Raw Material and Packing Material by using general pharmacopoeial test methods and using equipment like Autotitrator, KF Titrator, U.V. Spectrophotmeter, FTIR, HPLC
QC Micro: Code 3
Should be responsible for Environmental Monitoring (Air Sampling, Settle Plate, Surface Monitoring, Personnel Monitoring) / Water testing /Bio Assay / BET Test / Sterility Testing etc. For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential.
Interested candidates may send their updated CV along with current and expected CTC to email@example.com for Code 1 and Code 2 and to Ashok.Patel@zyduscadila.com for Code 3
Looking for Graduate / Post Graduate with 1 to 7 years of hands on experience for below mentioned openings:
Officer / Executive / Senior Executive / Assistant Manager
Responsible for warehouse management, dispensing of the raw materials, packing material etc., to qualify cold chambers / cabinets and its temperature mapping. For all above positions, candidate having exposure to SAP, regulatory requirement and cGMP/QMS knowledge is must along with pharma / biotech industry background
Interested candidates may send their updated CVs along with current and expected CTC to Milind.Shah@zyduscadila.com
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