Associate Manufacturing Nights C Position Available In Kent, Rhode Island

Salary Not Available Associate Manufacturing – Nights C
Amgen

Location:

West Greenwich, RI – 02817
Positions available: 1
Job #: 1210258

Source:

Meddevicejobs.com

Posted:

6/8/2025

Web Site:

www.meddevicejobs.com

Job Type:

Full Time (30 Hours or More) Job Requirements and Properties Help for Job Requirements and Properties. . Job Requirements and Properties Help for Job Requirements and Properties. .
Work Onsite
Full Time Schedule
Full Time
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Associate Manufacturing – Nights

C PUBLISHED

June 8, 2025 Onsite West Greenwich, Rhode Island EngineeringOperations

• 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. 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 (C shift)
• What you will do
• Let’s do this.

Let’s change the world. In this vital role you will join a team of impactful manufacturing associates that leverage adaptability, agility, teamwork, and curiosity. The Manufacturing Associate at Amgen supports the production process by operating equipment, maintaining production records, and adhering to safety and quality standards. They contribute to the overall efficiency of the manufacturing process.

Responsibilities Include:

+ Under general supervision, Associate will perform operations in the manufacturing area. + Operations will be performed according to Standard Operating Procedures (SOP’s) + Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP’s and technical reports. + Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. + May participate on cross-functional teams and represent the manufacturing teams. + Associate may also have the responsibility of owning deviations/CAPA’s. + In addition, Associate may identify, recommend and implement improvements related to routine functions. In this vital role you will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C 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 phase for this role (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 dedicated professional we seek is a great teammate with these qualifications. Additional Information Help for Additional Information. . Additional Information Help for Additional Information. .

• 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, chromatography, TFF 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
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