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Home / Job /  Vacancy for Fermentation, PDL, Production @ Lupin Pharmaceuticals

 Vacancy for Fermentation, PDL, Production @ Lupin Pharmaceuticals

 Vacancy for Fermentation, PDL, Production @ Lupin Pharmaceuticals


Lupin Pharmaceuticals, Inc. is the U.S. wholly owned subsidiary of Lupin Limited, which is among the top six pharmaceutical companies in India. Through our sales and marketing headquarters in Baltimore, MD, Lupin Pharmaceuticals, Inc.

Officer / Sr. Officer / Executive
Qualification : M.Sc. (Microbiology/Biotech)
Experience : Min. 2 to 8 years
(Experience in Pharma Industry. Fresher can also apply.)

(Sr. Officer/Officer)
Qualification : M Sc./B.Sc. – Analytical Chemistry / Organic Chemistry
Experience : Min. 2 to 5 years of relevant experience & knowledge in Process Development, Synthesis functions.

Production API
(Sr. Officer/Officer /Associate/Trainee)
Eligibility Criteria & Qualification : 01 To 06 Years M.Sc / B.Sc Chemistry / Diploma-Chemical.
Desired Exposure In : Responsibility includes adherence to SOP’s/to meet production targets, maintain safety practices. Able to handle and analyse process problems in manufacturing. Experience in API manufacturing with cGMP, SAP knowledge Sound knowledge of operations of centrifuge/reactors etc.

Highest degree must have at least 60 % marks or in case of 2nd Class, 5 years of experience post your Highest Qualification.

Kindly share your Resume first, once shortlisted we will call you for Interview Rounds

Location : Tarapur, Maharashtra

Last Date : 10th August, 2020


Apply for this position

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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