Walk-in interview for Zydus Biologics for the Production Department (DSP/USP/QMS) in Pune on 21st July, Sunday
USP Production:
Roles: Executive, Senior Executive, Assistant Manager Qualifications: M.Sc., B.Tech, B.E, M.Tech in Biotechnology/Biochemistry Experience: 2-10 yearsExecutive/Senior Executive/ Assistant Manager: Executive/Senior Executive/ Assistant Manager: M.Sc./ B. Tech/B. E/ M. Tech – Biotechnology/Biochemistry with 2 – 10 years of experience in handling of large-scale mammalian cell culture (SS bioreactor), media/feed preparation and its filtration. The job requires readiness of bioreactor and associated vessels (CIP, FIT, PHT, SIP), operation of bioreactor & associated vessels, readiness and operation of centrifuge, clarification of cells for manufacturing of monoclonal antibodies/ bio therapeutic protein.
DSP Production:
Roles: Executive, Senior Executive, Assistant Manager Qualifications: M.Sc., B.Tech, B.E, M.Tech in Biotechnology/Biochemistry Experience: 2-10 yearsExecutive/ Senior Executive/ Assistant Manager: M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 2-10 years of experience in downstream purification process for recombinant products, TFF system, chromatography system, virus filtration procedures and CIP/SIP of the equipment.
QMS Production:
Roles: Executive, Senior Executive, Associate Manager Qualifications: M.Sc., B.Tech, B.E, M.Tech in Biotechnology/Biochemistry Experience: 2-15 yearsExecutive/ Senior Executive/ Associate Manager: M.Sc./B.Tech/ B. E/ M. Tech – Biotechnology/Biochemistry Candidates with 2-15 years of experience in Preparation of risk assessment and investigation report. Meetings with cross functional team to identify the root causes of deviation, OOT and OOS. Initiation and/or review, closing of the QMS document such as deviation, change control and CAPA using Trackwise or similar software. Regular discussion with manufacturing team to reduce the human errors which leads to deviation. Preparation and/ or review of cGMP documents such as MFR, BMR, SOP etc.
For all above positions, candidates having exposure to regulatory requirement of documentation and cGMP/GLP is essential. Preference will be given to those who have thorough knowledge of all the manufacturing operations of Biosimilar products.
-------------------------------------------------------------------------------------------------------------
Note:
- All the employees will be working in shifts according to work allocation.
- The shift deployment for Male Candidates will be A/B/C. Candidates can walk in with a recent copy of their resume with copies of relevant qualification certificates/mark sheets, PAN Card, Aadhar Card, Latest increment letter, experience letter of previous organizations if any, and salary slips for the last 3 Months.