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.

Benefits

• Health insurance with dental and vision insurance options.
• Holiday pay.
• 401(k) program.
• Employee referral bonus program.
• The client retains the right to hire the contractor directly.