Manufacturing Process Tech-Manufacturing Services Nights (D Shift)

Amgen•West Greenwich, RI
•$54,411 - $73,615

About The Position

The Manufacturing Process Technician performs simple to moderately complex processes according to Standard Operating Procedures and Batch Records, covering bulk manufacturing in aseptic and non-aseptic environments. The role includes equipment cleaning, CIP and SIP of BDS vessels, raw-material weighing and dispensing, monitoring Delta-V recipes, sample handling, inventory activities, materials handling, and documentation. The technician follows current Good Manufacturing Practices (cGMPs) and completes calculations and physical tasks associated with bulk manufacturing. The position works on a shift team in 12-hour shifts, with a rotating schedule covering seven days per week and every other weekend off. During the initial 2–6 weeks of onboarding, the schedule is administrative, Monday through Friday, approximately 8 a.m. to 5 p.m. The posting describes the role as nights, although its stated rotating shift pattern is 7 a.m. to 7 p.m. A 15% shift differential is offered. The expected U.S. annual salary range, excluding Puerto Rico, is $54,411.05–$73,614.95. Actual salary varies based on relevant skills, experience, and qualifications. Amgen offers eligible employees a Total Rewards Plan and career development opportunities.

Requirements

  • High school diploma/GED plus one year of manufacturing or operations work experience, or military experience; alternatively, an associate's degree.
  • Ability to stand or sit for extended periods.
  • Ability to maintain focus during repetitive tasks over the course of a shift.
  • Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment according to procedures.
  • Basic understanding of measurements, calculations, and the metric system.
  • Ability to work effectively individually and as part of a team.
  • Ability to document process tasks in electronic batch records.
  • Ability to accept coaching and demonstrate learned, measurable improvement.
  • Ability to follow written procedures and recognize and report malfunctions.
  • Strong communication skills.
  • Ability to perform assignments with a high degree of focus and attention to detail.
  • Ability to work a 12-hour rotating shift schedule covering seven days per week.

Nice To Haves

  • Experience in a GMP or other regulated environment.
  • Demonstrated knowledge of GMP principles.
  • Drug substance manufacturing experience.

Responsibilities

  • Perform simple to moderately complex manufacturing processes according to Standard Operating Procedures and Batch Records.
  • Clean equipment, including Intermediate Bulk Containers (IBCs).
  • Perform CIP and SIP of BDS vessels.
  • Weigh and dispense raw materials.
  • Operate and monitor Delta-V recipes.
  • Collect, process, store, and deliver samples.
  • Manage and reconcile inventory.
  • Handle materials, including weighing and dispensing, and operate power industrial vehicles.
  • Adhere to current Good Manufacturing Practices (cGMPs).
  • Accurately complete process-associated documentation, make calculations, and perform physical tasks associated with bulk manufacturing.
  • Perform other duties as assigned.

Benefits

  • Health and welfare plans for staff and eligible dependents.
  • Retirement and savings plan with company contributions.
  • Group medical, dental, and vision coverage.
  • Life and disability insurance.
  • Flexible spending accounts.
  • Discretionary annual bonus program.
  • Stock-based long-term incentives.
  • Award-winning time-off plans.
  • Career development opportunities.
  • 15% shift differential.
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