Cell Therapy Lab Technologist

Actalent; United States; On-site; USD 33,000 - 34,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan pre-tax and/orR

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent is seeking a qualified candidate to join our GMP manufacturing and aseptic processing team in Hudson, WI. You will perform cleanroom manufacturing, operate specialized cell processing and counting equipment, and prepare reagents for production.

The role emphasizes strict GDP documentation, adherence to SOPs, and collaboration with Quality, Manufacturing, and R&D as the business scales from development to commercial manufacturing. Contract-to-hire with onsite work.”

Qualifications

• Bachelor's degree in Biology, Chemistry, or related field (Associates degree with relevant industry experience also considered).
• 1+ year of GMP-regulated pharmaceutical/biotech/medical device experience.
• Hands-on lab experience with aseptic technique, sample handling, reagent preparation, and documentation.
• Experience in cleanrooms or controlled manufacturing environments preferred.
• Strong attention to detail and ability to follow SOPs while maintaining accurate records.
• Excellent communication and documentation skills.

Responsibilities

• 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 GDP documentation in accordance with 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.

Skills

GMP experience

Aseptic technique

Lab equipment operation

Documentation practices

Attention to detail

Communication skills

Education

Bachelor's degree in Biology or Chemistry

Associates degree with relevant experience considered

Job description

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.

Workplace Type

This is a fully onsite position in Hudson,WI.

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)

Application Deadline

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

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.

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.