More jobs:
Manufacturing Associate
Job in
North Bothell Area, Snohomish County, Washington, 98021, USA
Listed on 2026-07-18
Listing for:
Spectraforce Technologies
Full Time
position Listed on 2026-07-18
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations, Production Associate / Production Line, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Work Location: Bothell, WA (100% Onsite)
Assignment Duration: 12 Months
Work Schedule: Sun - Alternate Wed, 11:00 AM - 11:30 PM
Work Arrangement: Onsite
Position Title: Manufacturing Associate
Position SummaryThe primary purpose of the Manufacturing Associate role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment.
Key Responsibilities- Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
- Adheres to Good Manufacturing Practices and standard operating procedures.
- Weighs and checks raw materials.
- Assembles, cleans and sanitizes process equipment, monitors processes.
- Completes work instructions and maintains clean room environment to comply with regulatory requirements.
- Trains for proficiency in the operation of primary production equipment within the assigned functional area.
- Trains for proficiency in process systems (i.e. Syncade MES and Oracle interfaces) and some supporting business systems (i.e. Oracle, ETQ, BMRAM etc.).
- Assist with the revision and or creation of process documents, such as SOPs and electronic work instructions.
- Assists in maintaining material and components inventory level.
- Supports safe work environment.
- Work in teams and have continual interaction with members of his/her team as well as other manufacturing teams throughout the production process in order to exchange information regarding the batch(s) in process.
- Works on assignments that are routine in nature where judgment is required in resolving problems and making routine recommendations.
- Associate's or Bachelor's degree in life sciences field is preferred. Minimum of high school diploma and/or equivalent combination of education and experience is required.
- 0-2 years of cGMP manufacturing experience is desired or equivalent in work experience or education.
- Proven experience working on teams where combined contribution, collaboration, and results were expected.
- Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications.
- Experience where attention to detail and personal accountability were critical to success.
- Demonstrates good interpersonal skills, is attentive and approachable.
- Maintains a professional and productive relationship with area management and co-workers.
- Must be able to stand/walk for extended periods of time.
- Must be able to work in a cleanroom environment and perform aseptic processing, which require gowning and PPE including safety shoes, safety glasses, aprons, face shields, PAPR, lab coats, full body gowns, hairnets, gloves, and hearing protection.
- Required to carry and/or lift up to 30 pounds several times per day.
- Required to push and/or pull up to 50 pounds several times per day.
- Position Handles Hazardous Materials.
Position Requirements
10+ Years
work experience
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