Manufacturing Process Tech - Solution Prep; Nights
Listed on 2026-10-04
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Manufacturing / Production
Manufacturing & Industrial Operations, Production Associate / Production Line
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.
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.
You will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7am-7pm with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off as well as receiving an added 15% shift differential. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).
Whatwe expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is an excellent teammate with these qualifications.
Basic Qualifications:
High school/GED + 1 year of Manufacturing or Operations work or military experience OR Associate's degree
Preferred Qualifications:
Experience in a GMP/ other regulated environment. Demonstrated knowledge of GMP principles. Drug substance manufacturing experience. 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. Strong communication skills. Ability to perform assignments with a high degree of focus/attention to detail.
From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
- 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 where possible. Refer to the Work Location Type in the job posting to see if this applies.
Salary Range 54,411.05
USD
-73,614.95 USD
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve…
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