Manufacturing Associate - Cell Therapy

We are seeking a Manufacturing Associate to support cell therapy production in a regulated biopharmaceutical manufacturing environment. This entry-level opportunity involves hands-on production activities, equipment preparation, GMP documentation, and teamwork in a cleanroom setting.

Key responsibilities:

• Perform routine manufacturing operations following approved SOPs and work instructions; Weigh and verify raw materials, assemble and sanitize production equipment, and monitor manufacturing processes; Maintain cleanroom conditions and follow cGMP and aseptic processing requirements; Complete production documentation and identify or escalate process deviations; Learn manufacturing systems, including electronic work instructions and production records; Support inventory management, process documentation, and safe manufacturing practices; Collaborate with manufacturing teams to maintain production quality and efficiency.
• Position details: Hourly rate: $21.14–$24.14; Contract length: 12 months with possible extension; Location: Bothell, WA; Work arrangement: 100% onsite; Schedule: Sunday–alternate Wednesday, 11:00 AM–11:30 PM, rotating schedule; W-2 contract position; No C2C options; No visa sponsorship.

Requirements

• Required: High school diploma or equivalent combination of education and experience; Ability to follow written manufacturing procedures and maintain accurate documentation; Strong attention to detail and ability to identify and escalate deviations; Good communication, interpersonal, and teamwork skills; Proficiency with basic computer applications; Ability to work onsite on the assigned rotating shift; Ability to work in a cleanroom environment using required gowning and PPE; Ability to stand or walk for extended periods, lift up to 30 pounds, and push or pull up to 50 pounds; Authorization to work in the United States without visa sponsorship.
• Preferred: Associate’s or Bachelor’s degree in life sciences; 0–2 years of cGMP manufacturing experience or equivalent relevant education or experience; Experience with SOPs, cleanroom operations, and aseptic processing; Experience in regulated environments, including regulatory inspections; Familiarity with Syncade MES, Oracle, ETQ, BMRAM, or similar systems; Experience with electronic manufacturing documentation, equipment management, or inventory management systems.