Somerset, NJ, US
156 days ago
Contract Analytical Research and Development Chemist
Contract Analytical Research and Development Chemist Location : Location US-NJ-Somerset Posted Date 4 months ago(6/11/2024 9:59 AM) Job ID 2024-3848 # of Openings 2 Category Analytical Research and Development Overview

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 Fifteen 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.

Responsibilities

This is a Contract Position - Hired through a Third Party Agency

 

Role Summary

 

The 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, dissolution, residual solvents testing, Particle size distribution of active pharmaceutical ingredients, excipients and finished dosage forms.

 

Essential Duties and Responsibilities

Perform Method Development/Method validation / stability testing, including report writing, for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, oral suspensions, Powder for oral suspensions and Nasal products with minimum supervisionSupport the Product Development team in developing new productsIdentification and characterization of the unknown impurities in the drug products and drug substancesSupport or independently perform Method Development/Method validation / stability testing for various dosage forms that includes Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, oral suspensions, Powder for oral suspensions and Nasal productsElemental impurity testing using ICP-MS / ICP – OES.Trouble shoot analytical issues to accomplish desired resultsOther duties as assigned Qualifications

Education & Experience

Bachelor's Degree in Chemistry, Biology, or related field, Master's Degree a plus3-10 years of experience working as an R&D Chemist for a pharmaceutical companyOperational and technical expertise in developing testing such as HPLC, GC, Dissolution, Particle size distribution, etc.Experience in pharmaceutical Method Development, Method Validation and stability testing.Capable of writing reports suitable for regulatory submission with minimum supervision.

Physical Requirements

This position may require lifting up to 20 pounds occasionally. Generally work is performed in a laboratory environment with chemicals, reagents and solvents.



Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law.

Confirm your E-mail: Send Email