Perrigo, headquartered in Ireland is One of the World’s leading Pharmaceuticals Manufacturers, a global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and prescription (Rx) pharmaceuticals, nutritional products, and active pharmaceutical ingredients (API), as well as receives royalties from Multiple Sclerosis drug Tysabri®. Nearly 13,000 Perrigo employees around the world commit themselves each day to the important mission of making Quality Affordable Healthcare Products. Over 3,000 unique formulations with over 18,000 SKUs, 50 Billion Oral solid and liquid/cream doses every year.
Post: Research Assistant - Stability - Analytical R&D
No.of Post: 01
Job Description
Responsible to Conduct analysis of stability samples.
Documentation of stability studies as per cGMP norms.
Preparing of the stability protocols, validation protocols and finished product specifications and SOPs, OOS and OOT documentation. Preparation of test methods and stability specifications,
Handle instruments, calibrations & records.
Candidate Profile
Well versed with usage of anlaytical instruments for anlaysis like HPLC, Disso, Stability. Aware of documentation practises as per regulatory norms of USFDA, cGMP, GLP, ICH Guidelines. Good at Communication.
Additional Information:
Experience: 3-5 years
Qualification: M.Sc, B.Pharm/M.Pharm
Location: Ambernath
Industry Type: Pharma
Functional Area: Analytical R&D
End Date: 26th January, 2017
Send your CV to deepali.dalvi@perrigo.com
with following details –
1. Current CTC -
2. Expected CTC -
3. Notice period -
4. Willingness for Ambernath, Mumbai location
Posted by,
Deepali Dalvi,
Perrigo Laboratories India Pvt. Ltd.
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