Manufacturing Associate - Cell Therapy

SOKOL GxP Services • Bothell, WA

7h • $19 - $24 • Onsite

About The Position

The Manufacturing Associate completes routine production assignments with high-quality, timely output in a cellular therapeutic manufacturing environment. Responsibilities include following written procedures and Good Manufacturing Practices, recognizing and escalating deviations from accepted practice, weighing and checking raw materials, assembling, cleaning, and sanitizing process equipment, monitoring processes, and completing work instructions. This role supports cleanroom compliance, aseptic processing, material and component inventory, process document updates, including SOPs and electronic work instructions, and a safe work environment. The Manufacturing Associate will train to proficiency on primary production equipment and manufacturing systems, including Syncade MES, Oracle interfaces, Oracle, ETQ, and BMRAM. Success in this role requires strong attention to detail, personal accountability, basic computer proficiency, clear communication, and the ability to work closely with a paired production teammate and other manufacturing teams. This position handles hazardous materials.

Requirements

• High school diploma or equivalent combination of education and experience
• Ability to work 100% onsite in Bothell, WA, Sunday through alternating Wednesday, from 11:00 AM to 11:30 PM
• Basic computer proficiency, including word processing, spreadsheets, and web-based applications
• Ability to follow written procedures, recognize deviations from accepted practice, and escalate concerns appropriately
• Strong attention to detail, personal accountability, teamwork, and basic communication skills
• Ability to stand and walk for extended periods
• Ability to work in a cleanroom and perform aseptic processing while wearing required PPE, including full-body gowning, gloves, hairnet, safety shoes, safety glasses, face shield, and PAPR as applicable
• Ability to lift and carry up to 30 pounds several times per day and push or pull up to 50 pounds several times per day

Nice To Haves

• Associate’s or Bachelor’s degree in Life Sciences
• 0–2 years of cGMP manufacturing experience or equivalent education or work experience
• Experience in a regulated manufacturing environment
• Biotech or clinical laboratory experience
• Experience with inventory management systems

Responsibilities

• Follow written procedures and Good Manufacturing Practices
• Recognize and escalate deviations from accepted practice
• Weigh and check raw materials
• Assemble, clean, and sanitize process equipment
• Monitor processes
• Complete work instructions
• Support cleanroom compliance
• Perform aseptic processing
• Manage material and component inventory
• Update process documents, including SOPs and electronic work instructions
• Maintain a safe work environment
• Train to proficiency on primary production equipment and manufacturing systems

Benefits

• 401(k)
• health insurance (incl. Dental and Vision)
• paid holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED