Intas Pharmaceuticals Ltd, Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors.
opportunities with Intas Pharmaceuticals
Walk In Drive at Pharmez, Ahmedabad.
Position: Executive to Sr. Executive
Department: Quality Control – Supervisor
Qualification: M.Sc / B.Pharma / M.Pharm
Experience: 5 to 9 Yrs.
Roles & Responsibilities
- Supervisor: To verify sequence before start of analysis. Controlling human error. Trouble shoot the instrument & method of technique. Reduction of unconfirmed OOS/OOT.
- Review of calibration & qualification activities of QC.
Positions: Executive to Sr. Executive
Department: Quality Control (QC – FG / Stability / AMV)
Qualification: M.Sc / B.Pharma / M.Pharm
Experience: 2 to 12 Yrs.
Roles & Responsibilities
- Analyst: Finished, AMV & Stability Section. Knowledge of Instrument – HPLC/GC. Preferably know-how of Chromeleon Software.
Positions: Executive to Executive
Department: Quality Control MICRO (Microbiology)
Qualification: M.sc – Micro
Experience: 2 to 7 Yrs.
Roles & Responsibilities
- Analyst: Having exposure related Environment Monitoring in formulation, Water analysis, Various Microbiology test like sterility, BET, MLT etc.
- Having exposure related to regulatory plants and basic knowledge of GLP & GMP.
- Ready to work in rotational shift.
Walk-in Interview details
Date: Thursday, 5th October 2023
Time: 09:00 AM to 02:00 PM
Venue: Intas Pharmaceutical Limited, Plot No. 05 to 14, Pharmez, Dist – Ahmedabad.
Note:
- Please carry your updated resume all educational, experience & salary documents
- Candidates who have appeared for an interview at Intas in the last six months arc requested not to apply
- Candidates must be open to work in shift duties and have pharma experience in regulated plant like USFDA, MHRA should apply.
