Method Development Chemist

The Analytical Chemist will collaborate with a project team of chemists in a laboratory setting to analyze and develop HPLC and GC methods. These methods are used for assays, impurity analysis, dissolution, residual solvents testing, and particle size distribution of active pharmaceutical ingredients, excipients, and finished dosage forms. Responsibilities Perform Method Development/Method Validation/Stability Testing for various dosage forms including Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, Oral Suspensions, Powder for Oral Suspensions, and Nasal Products with minimal supervision. Support the Product Development team in the creation of new products. Identify and characterize unknown impurities in drug products and substances. Conduct Elemental Impurity Testing using ICP-MS/ICP-OES. Troubleshoot analytical issues to achieve desired results. Write reports suitable for regulatory submission with minimal supervision. Perform other duties as assigned. Essential Skills Bachelor's Degree in Chemistry, Biology, or a related field; a Master's Degree is a plus. 3-10 years of experience as an R D Chemist in a pharmaceutical setting. Operational and technical expertise in HPLC, GC, Dissolution, and Particle Size Distribution. Experience in pharmaceutical Method Development, Method Validation, and Stability Testing. Additional Skills & Qualifications Capable of writing comprehensive reports for regulatory submissions with minimal supervision. Work Environment This role is based in Somerset, New Jersey, within a laboratory environment that involves working with chemicals, reagents, and solvents. The position may require occasional lifting of up to 20 pounds. The location serves as one of the fifteen global commercial manufacturing sites and houses additional Research and Development teams