Walk In Interview 4th Sept 2022 for M.Sc, B.Pharma, M.Pharma At Intas Pharmaceuticals. Intas is one of the main global drug definition advancement, assembling and showcasing organizations on the planet. It has been developing at around 25.5% CAGR throughout recent years and crossed the $1.9 billion imprint in the past monetary year.
Intas Pharmaceuticals Ltd invites Experienced, Dynamic & Self-Motivated Professionals for the below positions at the Ahmedabad location.
Intas Pharmaceuticals Ltd is recruiting for the accompanying positions:
-QA (IPQA, Equipment Qualification, Documentation)
-Solid Oral (Manufacturing and Packing)
-Parenteral (Manufacturing & Packaging)
-Quality Control
Refer Notification & all relevant information below. Interested and qualified applicants can attend at scheduled time.
Opportunity subtleties:
Department:QA, QC, Solid Oral, Parenteral (Manufacturing & Packaging)
Post Name: Officer/Executive
Capability: M.Sc, B.Pharma, M.Pharma
Experienced:01 to 6 years
Set of working responsibilities: Intas Pharmaceuticals Ltd Hiring For Officer/Executive !
Significant Details :
Place: Ahmedabad
Walk in Interview Date: 4th Sept 2022,
Time: 09:30 AM to 5:00 PM
Walk In Address:- Baroda Production Council, Productivity House, BPC Road, Alkapuri, Vadodara – 390007
Choice Process: The determination will be based on Interview.
Set of working responsibilities:
1. Officer/Executive
Department: QA (IPQA, Equipment Qualification, Documentation)
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 2 – 7 Years in IPQA, Equipment Qualification, documentation in Solid Oral & Injectable facility.
2. Officer/Executive
Department: Solid Oral (Manufacturing & Packaging)
Qualification: B.Pharm/ M.Pharm
Experience: 2 – 7 Years in Granulation, Compression & Coating activities for Manufacturing & Primary & Secondary line activities for packaging
3. Officer / Executive
Department: Parenteral (Manufacturing & Packaging)
Qualification: 2 – 7 years in Batch manufacturing, Aseptic Area, LYO (Freeze Dryer), Autoclave area supervision & documentation activities for Manufacturing & Parenteral line Packaging & Documentation activities for packaging
4. Officer / Executive
Department: QC (Finished Product, Stability)
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 2 – Years in the operation of HPLC, GC & experience to perform method validation/transfer
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