Contract Analytical Research and Development Chemist

2 months ago


Somerset, New Jersey, United States Lupin Pharmaceuticals Full time

About Lupin Pharmaceuticals

Lupin Pharmaceuticals is a leading global pharmaceutical company that is committed to delivering high-quality medicines to patients around the world. Our company 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.

Our Research and Development Team

Our Research and Development team is responsible for developing new products and improving existing ones. We are a people-focused organization that is centered around making a positive impact on our customers. We believe that dollars are not a measure of success, but rather the people we help along the way.

Job Summary

The Analytical Research Scientist 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.

Key Responsibilities

  • Perform method development, method validation, and stability testing, including report writing, for various dosage forms, including tablets, hard gelatin capsules, oral/topical liquids, oral suspensions, powder for oral suspensions, and nasal products, with minimum supervision.
  • Support the Product Development team in developing new products.
  • Identify and characterize unknown impurities in drug products and drug substances.
  • Support or independently perform method development, method validation, and stability testing for various dosage forms, including tablets, hard gelatin capsules, oral/topical liquids, oral suspensions, powder for oral suspensions, and nasal products.
  • Perform elemental impurity testing using ICP-MS/ICP OES.
  • Troubleshoot analytical issues to achieve desired results.
  • Other duties as assigned.

Qualifications

  • Bachelor's degree in chemistry, biology, or a related field; master's degree a plus.
  • 3-10 years of experience working as an R&D chemist for a pharmaceutical company.
  • Operational 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.
  • Ability to write 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.



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