Associate Manufacturing AME Nights - West Greenwich RI

VetJobs; West Greenwich (RI); Vor Ort; USD 90.000 - 110.000; Vollzeit

Zusammenfassung

Amgen is seeking an Associate Manufacturing - Nights to operate in Rhode Island, performing cell culture and purification tasks within multiple manufacturing areas. You will adhere to GMP, SOPs, CFRs, and batch record documentation while participating in an Agile Manufacturing Excellence team.

You will support cross-area manufacturing, learn various processes, and train staff as needed. A Bachelor’s degree and strong manufacturing experience are expected, with flexibility for night shifts and

Qualifikationen

• Bachelor’s degree or equivalent required.
• Strong understanding of GMP and manufacturing operations.
• Willingness to work nights and be flexible in a fast-paced environment.

Aufgaben

• Perform cell culture and purification tasks in manufacturing areas as part of Agile Manufacturing Excellence.
• Follow SOPs, MPs, JHAs, CFRs and document activities in batch records.
• Troubleshoot, review documentation, and assist in area deviations and audits.

Jobbeschreibung

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. 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.

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 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 elevate 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

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.

Auto req ID

486834BR

Minimum Education Required

Bachelors

Additional Qualifications/Responsibilities

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.
• 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

City*

West Greenwich

State*

Rhode Island

Job_Category

Health/Medical other

Job Code

Pharmaceutical Pharmaceutical

Affiliate Sponsor

Amgen

Salary Range

>$100,000