Job Details

Manufacturing Associate

?? Location: On-site: Richmond, CA

?? Type: Full-Time, Hourly, OnSite

?? Company: Confidential (Drug Testing Organization – Stealth Mode)

Peoplework LLC is hiring for our client, a rapidly growing drug testing organization operating in stealth mode, developing next-generation laboratory testing solutions. We are seeking a Manufacturing Associate to contribute to the commercial production of novel, medical diagnostic devices. You will operate equipment and assemble products in a clean or dry room environment while adhering to strict quality policies and procedures.

Immediate Needs

· Support build-out and setup of the AC line in H2 and base station line in SR1 (cleaning, staging, construction).

· Complete onboarding and training on core commercial processes (gowning/cleanroom, ESD, traceability, documentation, safety).

· Provide hands-on production support: kitting, basic assembly, in-process checks, packaging/labeling, and rework to meet early build schedules.

· Assist receiving and inventory organization: unpacking, labeling, cycle counts, sorting/disposing of legacy inventory, and accurate transactions.

· Perform miscellaneous lab/manufacturing support tasks as assigned (basic measurements, fixture setup, material prep).

Long-Term Needs

· Execute routine commercial manufacturing across H2, SR1, and TRT, meeting throughput, quality, and documentation requirements.

· Own daily inventory management (receiving support, material moves, cycle counts, Kanban/min-max restocking) to ensure uninterrupted production.

· Contribute to continuous improvement: propose/implement process and fixture improvements, participate in CAPA/deviation investigations, and support validation/scale-up.

· Cross-train across product lines and stations to provide flexible staffing and support future expansion.

Experience

· 2+ years of hands-on experience in a regulated manufacturing environment (medical device, diagnostics, biotech, or pharmaceutical).

· Experience performing assembly, kitting, labeling/packaging, and basic in-process inspection activities while meeting production schedules.

· Working knowledge of Good Manufacturing Practices (GMP) and/or Good Documentation Practices (GDP); experience completing batch records, travelers, or device history records (DHR) is a plus.

· Experience working in controlled environments (cleanroom, dry room, ESD-controlled area) and following gowning, line clearance, and contamination-control procedures.

· Comfortable using basic hand tools and measurement equipment (e.g., torque drivers, calipers, scales) and following work instructions/SOPs.

Knowledge & Skills

· Proficient in computer systems: Windows, Microsoft Word, Excel, PowerPoint and various file repositories.

· Ability to read and follow detailed instructions, maintain accurate records, and complete product inspections that meet all requirements.

· Understands and adheres to applicable production controls including but not limited to line clearance, gowning, ESD controls, PPE, etc.

· Good communication skills (written and verbal [English]), good penmanship, is detail oriented and ability to perform basic arithmetic.

· Understanding basic principles and function of common electronic and mechanical components.

Why Join Us

• Join a confidential, high-impact drug testing organization
• Play a key role in building manufacturing and validation processes from the ground up
• Work in a collaborative, fast-paced, and technically challenging environment
• Competitive compensation and benefits

Salary range: $25-$30/hour depending on experience

Due to the confidential nature of our work, additional details will be shared during the interview process.

Apply here or contact us directly to learn more.