QA,QC,IT,Eng Openings At Zydus Lifesciences Walk In 11th Sept 2022

QA,QC,IT,Eng Openings At Zydus Lifesciences Walk In 11th Sept 2022. Zydus Lifesciences Limited, formerly known as Cadila Healthcare Limited, is an Indian multinational pharmaceutical company headquartered in Ahmedabad, which is primarily engaged in the manufacture of generic drugs. It ranked 100th in the Fortune India 500 list in 2020.

Zydus Lifesciences Limited invites Experienced, Dynamic & Self-Motivated Professionals  for the below positions at the Ahmedabad location. 

Zydus Lifesciences Limited  is recruiting for the accompanying positions:

  - Quality Assurance 

   -Quality Control 

   -Information Technology

   -Engineering  

Refer Notification & all relevant information below. Interested and qualified applicants can attend at scheduled time.

Opportunity subtleties:

Department: Quality Assurance/Quality Control/Engineering/Information Technology

Post Name: Senior Executive to Manager/Technician /IT CSV Engineer /Officer / Sr. Executive /Dy. Manager / Assoc. Manager/Officer Dy. Manager (IPQA & QMS)

Capability: B.Pharm,M. Pharm,B.sc,M.sc,B.tech,MCA,Diploma     

Experienced:03 to 8 years

Salary:5,00,000 - 12,00,000 P.A.

Set of working responsibilities: Zydus Lifesciences Limited Hiring For Senior Executive to Manager/Technician /IT CSV Engineer /Officer / Sr. Executive /Dy. Manager / Assoc. Manager/Officer Dy. Manager (IPQA & QMS) !

Significant Details :

Place: Ahmedabad

Walk in Interview Date: Sunday, 11th September 2022

Time:9.30 a.m. - 5.00 p.m.

Walk In Address:- BARODA PRODUCTIVITY COUNCIL 2nd Floor, Productivity House, Productivity Road, Alkapuri, Vadodara 390 007

Note:Candidate not able to attend the Walk-in may share their resume at below contact credentials manan.hathi@zyduslife.com ( Engineering and Information Technology). & Shiju.P.George@zyduslife.com(QA & QC).

Choice Process: The determination will be based on Interview.

Set of working responsibilities:

Below are the Departments and the respective details:

Quality Assurance:

Officer Dy. Manager (IPQA & QMS) B. Pharm / M.Sc. / M. Pharm with 2 to 6 Years of relevant experience of IPQA and manufacturing QMS related activities in Oral Solid Dosage Manufacturing facilities.

Quality Control:

Officer / Sr. Executive Quality Control (Analyst) B.Sc./B. Pharm/M.Sc. with 2 to 8 years of hands-on experience of analytical instruments like HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should have experience of RM analysis, analytical Method transfer/Method validation and GLP.

Dy. Manager / Assoc. Manager Quality Control (Reviewer) B.Sc./B. Pharm/ M.Sc. with 7 to 12 years of experience of Analytical data Review of Raw material & Method transfer/Method validation section.

Engineering:

Technician Diploma/ITI with 3 to 8 years of experience in HVAC + BMS, HT, LT panels routine Operations, experience in Operations of Air Compressor, Chiller and Water system. Experience in OSD Process Equipment Maintenance. Experience in Instrument Sensors controls, Machine Operation, PLC, HML, SCADA, and experience in Calibration activity.

Senior Executive to Manager B.E / B.Tech (Mechanical/ Instrumentation/ Electrical/ Civil) with 4 to 15 years of experience in Scheduling and execution of preventive maintenance activities of OSD Process Equipment, HVAC + BMS Operations HT, LT panels, Installation and Upgradation. Scheduling and execution of preventive maintenance and In-house Calibration as well as external calibration activities. Maintenance of Air Compressor, Chiller and Water system. Knowledge of PLC,SCADA, HLM required.

Information Technology:

IT CSV Engineer - Diploma. / B.E/ B.Tech/ MCA with 4 to 8 years of experience in IT department. Should have exposure of User Management (Q.C. /Manufacturing/ Engineering /Warehouse /Packing), GxP Systems, Desktop policy and CFR part 11 requirement. Preparation, Review and/or execution of validation documents and SOPs. Knowledge of Documentum, Trackwise and other quality software also required. Exposure to Pharma industry is mandatory.

For all the positions, it is essential for candidates to have exposure in regulatory requirements of documentation and cGMP/GLP. Interested candidates please Walk-in for an interview along-with their updated Resume, Salary proof and relevant documents as per the schedule.