What are the responsibilities and job description for the Analytical Development, Quality Control Scientist position at EPM Scientific?
Are you looking for a partner to bring your pharmaceutical innovations to life? We are working with a leading Contract Development and Manufacturing Organization (CDMO) to make that happen for you. This company provides comprehensive services from initial drug development to commercial production, ensuring the products reach the market efficiently and effectively.This team of experts is dedicated to advancing the pharmaceutical projects with cutting-edge technology and innovative solutions.State-of-the-art manufacturing facilities to ensure the highest quality and compliance standards.From concept to commercialization, this company will provide tailored solutions to meet every unique need.Position : Analytical Development and Quality Control ScientistLocation : San DiegoAs an Analytical Development and Quality Control Scientist, you will play a crucial role in ensuring the quality and efficacy of the pharmaceutical products.Responsibilities : Create and optimize methods to support the selection and development of drug candidates.Transfer and validate analytical methods at third-party laboratories to ensure consistency and reliability.Oversee testing activities for drug products, active pharmaceutical ingredients (APIs), and raw materials at external contract research organizations (CROs).Conduct tests to support research and manufacturing, including release, stability, and characterization studies.Prepare, review, and evaluate scientific and technical protocols, reports, and quality control documents.Collaborate with QA, Regulatory, and Manufacturing departments to monitor and evaluate quality-related events such as out-of-specification results, deviations, and change controls.Requirements : Ph.D. in Analytical Chemistry, Biochemistry, or a related discipline.Minimum of 3 years of experience in pharmaceutical or biotech analytical development.Expertise in a variety of analytical techniques (e.g., HPLC, LC-MS, IR).Strong communication skills and fluency in English.Experience in a quality control environment and familiarity with regulatory guidelines.#J-18808-Ljbffr
