Intas Pharma-Walk in for Quality, Production Department on 24 Sept, 2023 

Intas Pharma-Walk in for Quality, Production Department on 24 Sept, 2023 

 

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.

Walk-In Drive at Indore – Quality & Injectable Production Department

Senior Officer – Executive
Department : QA -Validation & Qualification (Injectable)
Qualification : M.Sc. / B.Pharm / M.Pharm
Experience : 03 to 07 years
• Process and Cleaning validation, protocol report and risk assessment
• Equipment qualification documents (URS, FAT, SAT, DQ, IQ, OQ, PQ) & Compliance mgt.
• SME in HVAC validation, Equipment Qualification

Officer – Senior Officer

Department : Injectable / Parenteral (Manufacturing)
Qualification : B.Pharm / M.Pharm
Experience : 02 to 05 years
• Exposure to work in Bulk Manufacturing / Mfg skid with multiple vessel / NDDS area, Aseptic filling SVP, Lyophilization, Media fill, Qualification, QMS

Job Location : Intas Pharmaceuticals Ltd. Matoda – Ahmedabad, Gujarat.

Walk in Interview
Date : 24th September, 2023 (Sunday)
Time : 10:00 am to 05:00 pm
Venue : Papaya Tree Hotel, Indore A.B. Road, Indore Mega City Cir, Indore, Madhya Pradesh 453331

Job Category: pharma
Job Type: Full Time
Job Location: Ahmedabad

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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