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Associate Manufacturing - Nights; D shift

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Amgen SA
Full Time position
Listed on 2026-07-10
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Associate Manufacturing - Nights (D shift)
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.

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.

Associate Manufacturing - Nights What you will do

Let’s do this. Let’s change the world. 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.

Responsibilities Include:

  • 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 SOP's and performing LEAN functions.

  • Identify, recommend, and implement improvements related to routine functions.

In this role, you will be expected to work a 12‑hour shift (7PM‑7AM) on a rotating schedule (D‑ Shift). This includes extra benefits such as receiving an added 15% shift differential, and also getting premium pay for any Sundays worked. The schedule during the initial on‑boarding/training phase (2‑6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

What we expect of you

We 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

Preferred Qualifications:
  • 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 V

  • Experience with lab equipment/testing

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, we’ll 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…

Position Requirements
10+ Years work experience
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