Sr Associate Quality Control - West Greenwich, RI

Job Description ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr Associate Quality Control What you will do Let's do this. Let's change the world. In this vital role you will complete and review analytical testing in our cGMP laboratory. The role will be on-site based out of Amgen Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing. Responsibilities include: Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations Operate laboratory equipment and instrumentation Performs review and approval of assays, documents and records Supports Continual Improvement initiatives Alerts management of quality, compliance, supply and safety risks Participate in laboratory investigations Perform general laboratory housekeeping activities Completes required assigned training to permit carry through of required tasks Performs additional duties as specified by management Additional Qualifications/Responsibilities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek thrives in a fast paced environment and possesses these qualifications. Basic Qualifications: High school diploma / GED and 4 years of Quality or Operations experience OR Associate's degree and 2 years of Quality or Operations experience OR Bachelor's degree and 6 months of Quality or Operations experience OR Master's degree Preferred Qualifications: 1-2 years' experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing Demonstrated experience in laboratory investigations, method validation, audits, QC processes Ability to interpret scientific data Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction Strong communication skills (both written and oral), facilitation and presentation skills GMP/GDP experience Salary Range 83,951.00 USD - 100,822.00 USD

Created: 2026-03-04