Sobre este puesto de Manufacturing Associate - Cell Therapy en SOKOL GxP Services
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.