Cell Therapy Lab Technologist

Aseptic Processing | Cell Therapy | Biomanufacturing | Career Growth

Join a cutting-edge biotechnology organization developing innovative cell-based therapies aimed at improving the lives of individuals autoimmune diseases. This is an opportunity to work in a clinical-stage GMP manufacturing environment where you'll play a hands-on role in producing life-changing products while gaining exposure to advanced bioprocessing, quality systems, and cleanroom manufacturing.

What You'll Do

• Perform manufacturing and processing activities in a GMP cleanroom using aseptic and sterile techniques.

• Operate specialized laboratory and production equipment including cell processing, encapsulation, microscopy, and cell-counting systems.

• Prepare reagents, solutions, and materials to support manufacturing and laboratory operations.

• Accurately complete batch records, logbooks, and GMP documentation in accordance with Good Documentation Practices (GDP).

• Support quality initiatives, deviation investigations, environmental monitoring, and inspection readiness activities.

• Analyze production and laboratory data to support troubleshooting, process optimization, and continuous improvement efforts.

• Collaborate with Quality, Manufacturing, and R&D teams as the organization scales from development to commercial manufacturing.

• Maintain strict compliance with GMP regulations, SOPs, and biosecurity requirements.

What We're Looking For

• Bachelor's degree in Biology, Chemistry, or a related science field (Associates degree with relevant industry experience also considered).

• 1+ year of experience in a GMP-regulated, pharmaceutical, biotech, or medical device environment.

• Hands-on laboratory experience with aseptic technique, sample handling, reagent preparation, and documentation.

• Experience working in cleanrooms or controlled manufacturing environments preferred.

• Strong attention to detail and the ability to follow SOPs while maintaining accurate records.

• Excellent communication and documentation skills.

Preferred Experience

• FDA-regulated manufacturing environments.

• Cell therapy, bioprocessing, biologics, or pharmaceutical manufacturing.

• Environmental monitoring, quality systems, and deviation investigations.

• Continuous improvement and process optimization initiatives.

Work Environment

This role is based in a state-of-the-art GMP manufacturing facility and requires work in a cleanroom environment with full sterile gowning and adherence to strict aseptic and biosecurity protocols. The schedule is typically Monday-Friday, approximately 6:30 AM-4:00 PM, with occasional weekend coverage as needed.

If you're looking to build a career in biotechnology, biomanufacturing, or cell therapy while making a meaningful impact on patients' lives, we'd love to hear from you.

Job Type & Location

This is a Contract to Hire position based out of Hudson, WI.

Pay and Benefits

The pay range for this position is $24.00 - $25.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Hudson,WI.

Application Deadline

This position is anticipated to close on Oct 23, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.