Sr Specialist QA - Compliance Employer Amgen Location West Greenwich, Rhode Island Start date Sep 9, 2026 View more categories View less categories Discipline Clinical , Clinical Medicine , Regulatory , Legal/Compliance Required Education High School or equivalent Position Type Full time Hotbed Pharm Country , Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll 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, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Sr Specialist QA - Compliance What you will do Lets do this. Lets change the world. In this vital role you will coordinate all site logistics for regulatory inspections, corporate audits, internal audits, and customer audits across both manufacturing facilities. Also serve as a primary site coordinator for inspection readiness activities, including planning rooms, schedules, escorts, subject matter expert support, document retrieval processes, communications, and daily inspection management.

Key Responsibilities:

Partner across functions to maintain a continuous inspection-ready state for a multi-product GMP manufacturing operation. Develop, maintain, and continuously improve site inspection readiness programs, tools, trackers, playbooks, and governance processes. Coordinate cross-functional readiness plans for upcoming Health Authority inspections and major audits, including mock inspections, war-room preparation, document review, and interview readiness. Support inspection and audit strategy for new product introductions to ensure new processes, facilities, systems, documents, and personnel are inspection ready prior to implementation and filing-related activities. Ensure inspection-related commitments, actions, and deliverables are clearly assigned, tracked to completion, and escalated as needed. Facilitate cross-functional alignment on inspection narratives, site presentations, supporting data packages, and response coordination. Support preparation and maintenance of core inspection readiness content, including site overviews, facility maps, product flow summaries, SME rosters, document inventories, and inspection support tools. Coordinate document management and retrieval processes to support efficient and controlled responses during inspections and audits. Monitor readiness of quality systems and operational processes that are commonly scrutinized during inspections, including deviations, CAPAs, change control, complaints, training, validations, document management, and data integrity controls. Identify gaps, risks, or weak points that may affect inspection outcomes and work with functional owners to drive timely remediation. Support site self-assessments and gap assessments against cGMP requirements, internal standards, and regulatory inspection trends. Develop and sustain close working relationships with internal stakeholders and external business partners, to ensure aligned and effective audit and inspection support. Ensure lessons learned from prior inspections, audits, commitments, and industry enforcement actions are incorporated into site readiness activities. Track regulatory commitments and support timely follow-up to ensure inspection observations, actions, and commitments are completed and sustainable. Provide compliance support during inspections, including schedule management, room coordination, request tracking, communication support, and facilitation of cross-functional issue resolution. Support drafting, coordination, and review of inspection responses and related action plans, as applicable. Escalate significant quality, compliance, supply, and inspection readiness risks to site quality and senior leadership. Support continual improvement initiatives that strengthen site quality culture, inspection readiness capability, and execution discipline. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a collaborative leader with these qualifications. Basic Qualifications High school diploma / GED and 12 years of regulatory compliance experience OR Associates degree and 10 years of regulatory compliance experience OR Bachelors degree and 6 years of regulatory compliance experience OR Masters degree and 4 years of regulatory compliance experience OR Doctorate degree and 2 years of regulatory compliance experience Preferred Qualifications Bachelors Degree in Life Sciences or Engineering Experience with leading and/or participating in key roles to prepare for, execute and/or respond to outcomes from Health Authority inspections Experience in auditing and/or defending processes, procedures and decisions during Health Authority inspections 7+ years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical industry with progressively increasing responsibility and demonstrated experience in compliance, data analysis, project management, and quality systems Experience managing staff and/or leading cross-functional teams, projects and/or programs Thorough working knowledge of EU and US Good Manufacturing Practices (cGMPs) Thorough understanding of quality management systems and quality control processes related to bulk drug substance for commercial operations Previous exposure to bulk drug substance manufacturing and quality assurance processes Demonstrated ability to work autonomously, present data in an organized and logical manner and an ability to communicate effectively Demonstrated ability to navigate through ambiguity and provide a structured problem-solving approach Track record of building or participating as a member of successful teams Demonstrated ability to coordinate and lead cross-functional project teams to deliver to expectations and on schedule What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Company We are all different, yet we have this in common: our mission to serve patients. This sense of shared purpose is key to our becoming one of the world's leading biotechnology companies. It guides us as we continue to launch new medicines and reach millions of patients worldwide. We live the mission. We win together. We thrive on continual challenge. Our team of 22,000+ scientists and professionals worldwide bring distinct perspectives and experiences to all we do. We leverage our global talent to achieve together—to research, manufacture and deliver ever-better products and greater depth to our mission. At Amgen, there is a strong correlation between our high level of diversity and performance. Because addressing issues with a wider range of perspectives and approaches leads to more creative problem-solving. Together, we're transforming the promise of science and biotechnology into therapies that have the power to restore health. Connect with us to explore how you can Win, Live, and Thrive at Amgen.

Company info Website http:

//careers.amgen.com/ Phone 805-447-1000 Location Corporate Headquarters One Amgen Center Drive Thousand Oaks California 91320-1799 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs QA, Shop Floor Specialist II Raritan, New Jersey Principal Scientist- Quality Control Microbiology Lead Baltimore, MD (CW) QC Analyst Contract Novato, California