Zydus Inviting candidates for a walk in Interview for formulation manufacturing plant on 11th September, 2022 (QA, QC, Engineering, IT)
On Sunday, 11th September, 2022 from 9:30 am to 5 pm at Vadodara
Quality Assurance
Officer – Dy. Manager (IPQA & QMS): B. Pharm / M.Sc. / M. Pharm with 3-9 years of relevant experience in IPQA and manufacturing QMS related activities in Oral Solid Dosage.
Quality Control
Officer/Sr. Executive – Quality Control (Analyst): B.Sc./B. Pharm/M.Sc. with 2-8 years of hands-on experience in analytical instruments like HPLC, GC, dissolution apparatus and UV-visible spectrometer. Should have experience in RM analysis, analytical method transfer / method validation and GLP.
Dy. Manager / Assoc. Manager – Quality Control (Reviewer): B.Sc./B. Pharm / M.Sc. with 7-12 years of experience in analytical data review of raw material & method transfer / method validation section.
Engineering
Technician Diploma / ITI with 3-8 years of experience in HVAC+BMS, HT, LT panels routine operations. Candidates should be able to operate air compressor, chiller and water system. They should have experience in OSD process equipment maintenance, instruments like sensor control, machine operation, PLC, HML, SCADA, and experience in calibration activities.
Senior Executive to Manager: B.E. / B.Tech (Mechanical / Instrumentation / Electrical / Civil) with 4-15 years of experience in scheduling and executing preventive maintenance activities of OSD process equipment, HVAC + BMS operations HT, LT panels, installation and upgradation. The role also requires scheduling and executing preventive maintenance, in-house Calibration as well as external calibration activities, maintaining air compressor, chiller and water system. Candidates should also have knowledge on PLC, SCADA, HLM.
Information Technology
IT CSV Engineer: Diploma / B.E. / M.C.A. with 4-8 years of experience in IT
department. Candidates should have experience in user management (Q.C. / manufacturing/ engineering/warehouse / packing), GxP systems, desktop policy and CFR part 11 requirement. The job requires preparation, review and execution of validation documents and candidates should be thorough with the SOPs. They are also required to possess knowledge on documentum, trackwise and other quality softwares.
For all the above positions, it is essential for candidates to have exposure to regulatory requirements of documentation and cGMP/GLP. Interested candidates can walk in for an interview alongwith their updated CVs, salary proofs and relevant documents. Candidates can also share their CVs with [email protected] & [email protected]
Venue : Baroda Productivity Council, 2nd Floor, Productivity House, Productivity Road, Alkapuri, Vadodara – 390 007
