Associate Manufacturing AME - Nights

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.

Associate Manufacturing - Nights

What you will do

Lets do this. Lets change the world. In this vital role you will perform operations within multiple Manufacturing areas, including cell culture and purification, at Amgen's innovative Rhode Island facility. This agile approach helps align staff capability with labor demand peaks across areas while building broader manufacturing experience. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), and to understand, follow, and document work in batch records.

Responsibilities Include

Perform cell culture, purification, weigh & dispense, and solutions batching tasks as part of an Agile Manufacturing Excellence team in two drug substance plants

Perform tasks in accordance with Standard Operating Procedures (SOPs), Manufacturing Procedures (MPs), Job Hazard Analysis (JHAs), and applicable Code of Federal Regulations (CFRs)

Perform and monitor critical manufacturing processes

Conduct basic troubleshooting and assist in the review of documentation for assigned functions.

May also have the responsibility of initiating and owning area deviations

Assist in the review of documentation for assigned functions, including routine area audits and batch records

Perform activities that may include rigorous and repetitive work

Work around high-pressure systems and occasionally around heavy equipment

Train staff on hands-on tasks, as needed

Serve as a safety representative, as needed

Provide operational feedback and escalate issues observed

Identify, recommend, and implement improvements related to routine functions

Ability to work with different teams in an ever-changing, fast-paced environment

Ability to maintain training and proficiency in supplemental assigned areas

Enthusiasm for learning the different manufacturing areas and technologies at ARI

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

Agile Workforce and Cross-Area Support

Support an agile manufacturing workforce by developing broader capabilities across assigned manufacturing areas and applying those skills where product demand, labor needs, and business priorities require. Based on training, qualifications, and operational needs, move between areas to help address periods of peak demand and maintain effective production support across AR5 and AR30 manufacturing areas.

Work collaboratively with area teams and Front-Line Managers (FLMs) to align assignments with campaign needs and defined work durations. Follow applicable training, qualification, GMP, and safety requirements when supporting work outside the primary area. Use cross-area experience to contribute to problem solving, build technical depth, and support continuous improvement.

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

Associates + 6 months of manufacturing or operations work experience OR

Bachelors Degree in a related field

Preferred Qualifications

Bachelors degree in Science or Engineering

Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.

Demonstrated foundational technical knowledge or transferable experience applicable to manufacturing, engineering, or operational environments.

Strong learning orientation with the ability to quickly develop technical proficiency in assigned areas.

Positive, collaborative attitude with a willingness to contribute to team success.

Ability to build effective working relationships across functions and with diverse stakeholders.

Demonstrated initiative by proactively seeking feedback, asking questions, and identifying learning opportunities.

Comfortable working in changing environments and adapting to evolving business priorities.

Strong organizational skills with the ability to remain focused on assigned responsibilities while managing competing priorities.

Demonstrated commitment to following established operational standards and procedures.

Ability to represent the organization professionally through collaboration, accountability, and customer-focused behaviors.

Willingness to accept coaching, demonstrate humility, and continuously improve through feedback.

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

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, 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, including remote and hybrid work arrangements, where possible

Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

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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.