Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women’s health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of twelve commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.

Analytical Chemist  will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.

THIS IS A CONTRACTUAL POSITON - being hired through a 3rd Party 

THIS POSITON IS FOR 2nd SHIFT  2:30pm -11pm

Essential Duties and Responsibilities

• Method Development/Method validation development, including report writing, for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids and Powder for oral suspensions with minimum supervision
• Support the Product Development team in developing new products
• Perform Method verifications and alternate vendor qualifications.
• Perform physical testing and dissolutions for the finished product dosage forms
• Trouble shoot analytical issues to accomplish desired results
• Other duties as assigned

Education & Experience

• Bachelor's Degree in Chemistry, Biology, or related field, Master's Degree a plus
• 2-5 years of experience working as an R&D Chemist for a pharmaceutical company
• Operational and technical expertise in developing testing using HPLC, GC, Dissolution, etc
• Experience in pharmaceutical Method Development and Method Validation
• Capable of writing reports suitable for regulatory submission with minimum supervision
• Strong knowledge in Empower 3 software and work in the GMP environment

Physical Requirements

The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in a laboratory environment

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