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Amgen - West Greenwich, RI

posted 4 months ago

Full-time - Entry Level
Remote - West Greenwich, RI
Chemical Manufacturing

About the position

The Manufacturing Process Technician - Nights at Amgen plays a crucial role in the biotechnology sector, focusing on bulk manufacturing processes in both aseptic and non-aseptic environments. This position involves performing a variety of tasks according to established Standard Operating Procedures (SOPs) and Batch Records, ensuring compliance with Good Manufacturing Practices (cGMP). The technician will work in a team setting on a rotating 12-hour night shift, contributing to the company's mission of serving patients worldwide.

Responsibilities

  • Perform simple to moderately complex processes according to Standard Operating Procedures and Batch Records.
  • Clean equipment and parts using manual and automated methods.
  • Assemble, disassemble, clean, and steam portable and stationary tanks and associated equipment.
  • Operate and monitor clean systems, autoclaves, and processing equipment.
  • Collect, process, store, and deliver samples.
  • Reconcile product and components accurately.
  • Prepare and transfer solutions.
  • Handle materials, including weighing and dispensing, and operate power industrial vehicles.
  • Adhere strictly to current Good Manufacturing Practices (cGMP) and complete process-associated documentation accurately.

Requirements

  • High school diploma or GED with 1 year of Manufacturing or Operations work or military experience, or an Associate's degree.
  • Experience in a GMP or other regulated environment is preferred.
  • Demonstrated knowledge of GMP principles is preferred.
  • Drug substance manufacturing experience is preferred.
  • Ability to stand or sit for extended periods of time.
  • Ability to maintain focus during repetitious tasks over the course of a shift.
  • Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment per procedures.
  • Basic understanding of measurements, calculations, and the metric system.
  • Ability to work effectively in both individual and team settings.
  • Ability to document process tasks in electronic batch records.
  • Coachable and able to take coaching/critique and show measurable improvement.
  • Capacity to follow written procedures and recognize/report malfunctions.
  • Strong communication skills and attention to detail.

Nice-to-haves

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

Benefits

  • Comprehensive employee benefits package including health, dental, and vision coverage.
  • Retirement and Savings Plan with generous company contributions.
  • Life and disability insurance.
  • Flexible spending accounts.
  • Discretionary annual bonus program.
  • Stock-based long-term incentives.
  • Award-winning time-off plans and bi-annual company-wide shutdowns.
  • Flexible work models, including remote work arrangements.
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