Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, every day and everyone works to create a world of good health, happiness and hope.
Assistant Manger
Department : Quality Control
Section : QC-Shift In charge
Qualification : M.Sc / B.Pharma / M.Pharm
Experience : 12 to 16 Yrs
• Resource Allocation and Work Schedule planning Reduction of unconfirmed OOS /OOT. Exposure of CDS and Non CDS (Chromatographic Database Software). Must have worked in USFDA /MHRA/EU certified labs. Should have exposure of Dl and DG. Should of Handled team size of 10 to 15 employees. Should have exposure on Formulation like Solid, Injectable, Onco Product, etc.
Senior Executive
Department : Quality Control
Section : QC - Supervisor
Qualification : B.sc / M.Sc / B. Pharmacy/ M.Pharm
Experience : 07 to 12 Yrs
• To Verify sequence before start of analysis. Controlling the human errorTrouble shoot the instrument & method of technique. Reduction of unconfirmed OOS /OOT. Review of calibration & qualification activities of QC.
Officer to Senior Executive
Department : Quality Control
Section : QC-FG/ Stability /AMV
Qualification : B.sc / M.Sc / B. Pharmacy/ M.Pharm
Experience : 02 to 08 Yrs
• Finished, & Stability Section. Knowledge of Instrument - HPLC / GC. Preferably know-how of Chromeleon Software
Job location : INTAS PHARMEZ, AHMEDABAD
Walk in Interview
Date : 17th November, 2023 (Friday)
Time : 09:00 am to 05:00 pm
Venue : Intas Pharmaceutical Limited, Plot No 5 to 14, Pharmez, Sarkhej - Bavla Highway, At & Po : Motoda, Ta : Sanad, Dist: Ahmedabad - 328 210.
Please carry your updated resume all educational, experience & salary documents
Candidates who have appeared for an interview at Intas in the last six months are requested not to apply
Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.
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