Mfg Process Technician - Days

AmgenWest Greenwich, RI
Onsite

About The Position

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. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. 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. Manufacturing Process Technician - Days What you will do Let’s do this. Let’s change the world. In this vital role you will routinely perform simple to moderately-complex processes according to Standard Operating Procedure and Batch Records. Generally, this will include all aspects associated with bulk manufacturing in aseptic and non-aseptic environments.

Requirements

  • High school/GED + 1 year of manufacturing work or military experience OR Associate's Degree
  • 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 an individual and team setting.
  • Ability to document process tasks in electronic batch records.
  • Coachable, ability to take coaching/critique and show learned/measurable improvement.
  • Capacity to follow written procedures, recognize and report malfunctions.
  • Good communication skills.
  • Ability to perform assignments with a high degree of focus/attention to detail.

Nice To Haves

  • 1+ plus years of experience in a GMP/ other regulated environment.
  • Demonstrated knowledge of GMP principles.
  • Drug substance manufacturing experience.

Responsibilities

  • Equipment and parts cleaning using manual and automated methods and equipment
  • Set up and breakdown of single use materials
  • Weigh and dispense of raw materials
  • Operation and process monitoring of clean systems, autoclaves, and processing equipment
  • Sample collection, processing, storage and delivery
  • Product and component reconciliation
  • Solution preparation and transfer
  • Materials handling, weighing and dispensing, power industrial vehicle operation
  • Strict adherence to current Good Manufacturing Practices (cGMP's), responsible to accurately complete process-associated documentation, make calculations and perform the physical tasks associated with bulk manufacturing and other duties as assigned.

Benefits

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models, including remote and hybrid work arrangements, where possible
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