Job Description
SOKOL GxP Services is seeking a Manufacturing Associate to support cellular therapy production operations in Bothell, Washington. This is a 100% onsite position within a regulated cleanroom manufacturing environment.
The Manufacturing Associate will complete routine production assignments according to written procedures, Good Manufacturing Practices, and established standard operating procedures. The role requires close attention to detail, the ability to recognize and escalate deviations, and consistent collaboration with other manufacturing personnel.
Responsibilities include:
- Perform routine cellular therapy manufacturing activities according to written procedures and electronic work instructions.
- Follow current Good Manufacturing Practices, standard operating procedures, and regulatory requirements.
- Weigh and verify raw materials used in production.
- Assemble, clean, and sanitize manufacturing equipment.
- Monitor manufacturing processes and escalate deviations or concerns as appropriate.
- Complete work instructions and maintain a compliant cleanroom environment.
- Train toward proficiency in the operation of assigned production equipment.
- Train in manufacturing process systems, including Syncade MES and Oracle interfaces.
- Use supporting business systems such as Oracle, ETQ, and BMRAM.
- Support revisions or creation of SOPs, process documents, and electronic work instructions.
- Assist with maintaining appropriate inventory levels for materials and components.
- Work closely with a manufacturing partner and other teams throughout the production process.
- Exchange accurate information regarding batches in process.
- Support a safe, professional, and productive work environment.
- Proactively seek additional information and assignments when work is completed.
- Respond constructively to feedback and actively apply it to daily work.
This role requires frequent standing and walking, cleanroom gowning, aseptic processing, and the handling of manufacturing materials and equipment.
Requirements
Required Qualifications
- High school diploma or an equivalent combination of education and experience.
- Ability to follow detailed written procedures and escalate concerns or deviations when necessary.
- Ability to perform basic computer tasks using word-processing, spreadsheet, and web-based applications.
- Strong attention to detail and personal accountability.
- Ability to work effectively in pairs and as part of a manufacturing team.
- Clear basic communication and escalation skills.
- Willingness to receive feedback and actively apply it.
- Ability to multitask in a fast-paced manufacturing environment.
- Ability to work 100% onsite in Bothell, Washington.
- Ability to work the assigned shift: alternating Wednesday through Saturday, 5:00 a.m.–5:30 p.m.
- Ability to stand and walk for extended periods.
- Ability to work in a cleanroom environment and perform aseptic processing.
- Ability to wear required PPE, including safety shoes, safety glasses, aprons, face shields, powered air-purifying respirators, lab coats, full-body gowns, hairnets, gloves, and hearing protection.
- Ability to carry or lift up to 30 pounds several times per day.
- Ability to push or pull up to 50 pounds several times per day.
Preferred Qualifications
- Associate’s or Bachelor’s degree in life sciences.
- Up to two years of cGMP manufacturing experience.
- Experience in a regulated or controlled environment.
- Biotechnology, cellular therapy, clinical laboratory, or related laboratory experience.
- Experience with aseptic processing or cleanroom operations.
- Experience with inventory management systems.
- Familiarity with Syncade MES, Oracle, ETQ, or BMRAM.
- Previous experience working in teams where collaboration and combined results were expected.
Benefits
H ealth insurance, holiday pay, 401(k) program, referral program, and other benefits
Hourly rate, $: 17.28 - 22 (W-2 only, no C2C)
12-month contract with possible extension
Schedule: Wednesday - Saturday, 5:00 a.m.–5:30 p.m.
Target start date: July 6, 2026
