Associate Manufacturing

What You Will Do

• - Perform operations within Manufacturing, specifically purification, at Amgen's Rhode Island facility.
• - Apply Good Manufacturing Practices (GMP) and understand, follow, and document in batch records.
• - Work a 12-hour rotating schedule (7AM-7PM, two-week rotation; average 14 days on shift per month; every other weekend off).

• - Perform and monitor critical GMP manufacturing operations per SOPs.
• - Use and perform basic troubleshooting in electronic systems (MES, Delta V, ERP).
• - Execute routine validation protocols; draft and revise manufacturing procedures, SOPs, and technical reports.
• - Participate in and lead safety and quality initiatives.
• - Support Lean Manufacturing by identifying improvement opportunities and implementing solutions.
• - Work with diverse teams; escape issues appropriately.
• - Own corrective and preventative action and non-conformance records.

• - High school/GED + 2 years manufacturing/operations experience OR
• - Associate's + 6 months manufacturing/operations experience OR
• - Bachelor’s degree in a related field.

• - Knowledge of large-scale purification (chromatography, TFF, aseptic processing, etc.); large-scale cell culture.
• - CFR/regulatory knowledge; mechanical expertise on fed-batch equipment.
• - Knowledge of WIP lab equipment/computers with LIMS access;
  Trackwise technical writing.
• - Project management/presentation skills; basic statistical/math skills; GMP interpretation; analytical methods.
• - Experience with Delta V, RD's; lab equipment/testing.

• - Total Rewards Plan may include comprehensive benefits (retirement/savings, medical/dental/vision, life/disability, flexible spending), annual bonus/incentive, stock-based long-term incentives, time-off, and flexible work models where possible.