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 Formulation Development
No.of post: 01
Job Description
Providing technical support to product/process development and commercialization activities for new immediate release and modified release solid oral dosage, liquid oral dosage forms and semisolid topical dosage forms to facilitate “First-to-File” and “First-to-Market” corporate goals. Supports the manufacture of Pivotal/Registration lots for new products in the Product/Process Development Pilot Plant and Manufacturing facilities. Generate data, following established procedures and practices. Record, tabulate, summarize and report results to Senior Scientific staff. Prepare Master Batch records for Experimental , Pilot / Pivot, scale-up and process validation batches. Support hands-on formulation design, development and optimization with guidance. Execute stability studies as directed. Perform scientific experimentation testing new products in development. Contribute to the development and documentation of new experimental approaches. With guidance, supports effective problem solving, resolution and implementation of process improvements in designated day-to-day operations and participate in large scope product / process development and improvement projects. Communicates effectively to senior scientific staff and the wider development team and presents data at team meetings and departmental technical meetings. Ensure compliance with current Drug Enforcement Administration (DEA), current Good Manufacturing Practices (cGMP), Perrigo policies and Quality Systems, and all applicable regulatory agencies.
Candidate Profile
6-10 years of working experience
Additional Information:
Experience: 6-10 Years
Qualification: Master’s in Pharmacy (Pharmaceutics)
Location: Ambernath
Industry Type: Pharma Formulation
Functional Area: Formulation R&D
Last date: 30th November, 2015
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