Analytical Development, Scientist II

We are seeking a Scientist II to provide analytical support for multiple development projects within a cGMP-regulated environment . This role will be responsible for developing, validating, transferring , and executing analytical methods for APIs, intermediates, and raw materials . The ideal candidate will have hands-on experience with analytical instrumentation, strong documentation skills, and a solid understanding of pharmaceutical analytical chemistry. Responsibilities Develop, optimize, validate, and transfer analytical methods for raw materials, intermediates, and finished products. Perform analytical testing using techniques such as HPLC, GC, GC/MS, LC/MS, FTIR, titration, and particle size analysis. Collect, analyze, and document analytical data in compliance with cGMP requirements. Support method qualification, compound identification, purity, potency, and stability testing activities. Maintain accurate laboratory notebooks and technical documentation. Ensure compliance with cGMP, SOPs, and applicable regulatory requirements. Collaborate with cross-functional teams to support development, quality, and manufacturing objectives. Coordinate external analytical testing and support reference standard qualification activities as needed. Qualifications M.S. in Chemistry or a related scientific discipline with 2+ years of laboratory experience, or B.S. in Chemistry or a related scientific discipline with 6+ years of laboratory experience. Experience in pharmaceutical, API, or cGMP-regulated environments preferred. Hands-on experience with analytical instrumentation including HPLC, GC, LC/MS, GC/MS, and FTIR. #J-18808-Ljbffr Meet Life Sciences