Associate Manufacturing - Nights; D shift
Listed on 2026-07-14
-
Manufacturing / Production
Production QC/QA, Quality Engineering, Pharmaceutical Manufacturing
Location: West Greenwich
Join Amgen’s Mission of Serving Patients 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.
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, 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.
In this vital role you will perform operations within the Manufacturing area, specifically solutions, at Amgen's innovative Rhode Island facility. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), as well as understand, follow, and document in batch records.
- Perform batching and transfer of Buffers and Media in appropriate areas according to Standard Operating Procedures (SOPs).
- Follow and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
- Conduct basic troubleshooting and assist in the review of documentation for assigned functions.
- May also have the responsibility of initiating and owning area Deviations, revising SOPs and performing LEAN functions.
- Identify, recommend, and implement improvements related to routine functions.
Work a 12‑hour shift (7 PM–7 AM) on a rotating schedule (D‑Shift). This includes extra benefits, including a 15 % shift differential and premium pay for any Sundays worked. The schedule during the initial onboarding/training phase (2–6 weeks) will be administrative (Monday through Friday, approximately 8 AM to 5 PM).
What We Expect Of YouWe are all different, yet we all use our unique contributions to serve patients. The driven professional we seek is a self‑starter with these qualifications.
Basic Qualifications- High school/GED + 2 years of manufacturing or operations work experience OR
- Associate’s + 6 months of manufacturing or operations work experience OR
- Bachelor’s Degree in a related field
- Bachelor’s degree in Science or Engineering
- Knowledge of large‑scale biotechnology operations such as purification, cell culture, aseptic processing, etc.
- Knowledge of Single‑use Systems
- CFR and Regulatory knowledge
- Mechanical ability/expertise
- Basic statistical mathematical skills
- Ability to interpret and apply GMP knowledge
- Understanding of analytical methods for manufacturing area
- Demonstrated technical writing capability
- Able to demonstrate project management skills and presentation skills
- Ability to understand, apply and evaluate basic chemistry, biology and physical principles
- Basic troubleshooting skills on production equipment
- Experience with Delta VExperience with lab equipment/testing
We support your professional and personal growth and well‑being through competitive benefits and a collaborative culture.
- 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, and for field sales representatives, a sales‑based incentive plan
- Stock‑based long‑term incentives
- Award‑winning time‑off plans
- Flexible work models, including remote and hybrid work arrangements, where possible
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.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).