Scientist

The Analytical Development Scientist is responsible for performing laboratory testing on raw materials, in-process samples, and finished products, as well as supporting stability studies and validation activities for drug product development. This role operates in a cGMP environment and requires a strong understanding of pharmaceutical regulations and analytical best practices. Key Responsibilities Perform routine analytical testing, method validation, and process validation in accordance with SOPs, cGMP, GLP, GDP, and regulatory guidelines (FDA, DEA, OSHA) Follow applicable compendial and regulatory standards for analytical procedures, method development, validation, and transfer Troubleshoot laboratory methods and instrumentation, including HPLC and UPLC systems Utilize Empower 3 software to analyze, interpret, and report analytical data Complete assigned work efficiently while maintaining a strong focus on safety, quality, and timelines Requirements BS or MS in chemistry, organic chemistry, or biochemistry Minimum of 2 - 3 years relevant experience in an analytical laboratory Ability to think beyond routine analysis of samples to detect issues with the method, product, or instrumentation Basic knowledge of USP/NF, Product Stability requirements, and Process and Method validation. Ability to integrate into team-based projects Experience with laboratory instrumentation such as HPLC, Dissolution Bath, GC, Karl Fischer titrator, UV/Vis, and FT-IR Spectrometer. Strong interpersonal communication and writing skills Competency in Microsoft Office Suite Compensation: Ranges from $75,000 - $95,000 a year annual salary. Bonus opportunities are available. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role include: Benefit packages for this role may include healthcare insurance offerings and paid leave as provided by applicable law. #J-18808-Ljbffr Insight Global