Perrigo Labaoratories invites Scientist - ARD – Stability Document Reviewer | 3 Opening

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: Scientist - ARD – Stability Document Reviewer

No.of post: 03

Job Description
Reviewing all Stability documents involved in registration stability as per cGMP or SOPs for the projects and stability on timely basis. Should review all tests for the projects and associated documentation, the documents to be Attributable, Legible, Contemporaneous, Original and Accurate. Preparing the CoA’s/method validation and method transfer protocol and reports. Audit the lab as per schedule. Provide support for on job training of analytical instruments to new joinee’s. Participate in projects and laboratory system related meeting and provide the inputs. Responsible for analytical method development and analysis of finishing product as per cGMP.

Candidate Profile
Education : Master degree in Science and Pharmacy with specialization of Analytical
8-10 years of experience

Additional Information:
Experience: 8-10 Years
Qualification: M.Sc, M.Pharm
Location: Ambernath
Industry Type: Pharma
Functional Area: Analytical R&D
Last date: 30^th November, 2015