Lab Technician

Job Title: Lab Technician GMP ManufacturingJob Description

This Lab Technician role focuses on the manufacturing, processing, quality support, and distribution of porcine islet and encapsulated islet combination products within a GMP-regulated cleanroom environment. You will perform highly specialized laboratory and manufacturing activities, ensure product quality, support regulatory compliance, and consistently apply aseptic processing standards. Working within established SOPs and Good Manufacturing Practices (GMP), you will maintain accurate documentation, operate specialized laboratory equipment, contribute to quality initiatives, and support the daily operation of a growing GMP manufacturing facility that produces an innovative therapy for people with Type 1 diabetes.

Responsibilities

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

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

• Prepare reagents, solutions, and materials required for manufacturing operations and laboratory testing activities.

• Complete batch records, logbooks, deviation reports, and production documentation accurately, contemporaneously, and in accordance with Good Documentation Practices (GDP).

• Maintain compliance with GMP regulations, internal quality systems, and established SOPs throughout all manufacturing and laboratory activities.

• Collect, analyze, and summarize production and laboratory data to support process monitoring, troubleshooting, and continuous improvement.

• Support inspection readiness activities and contribute to regulatory compliance efforts for FDA-regulated manufacturing operations.

• Perform environmental monitoring activities within the cleanroom and controlled areas to ensure ongoing compliance with environmental and biosecurity standards.

• Collaborate with cross-functional teams to support the transition from R&D to full GMP manufacturing and to drive ongoing operational improvements.

• Uphold biosecurity standards, including adherence to site-specific access and contact requirements related to swine exposure.

Essential Skills

• Bachelors degree in chemistry, biology, or a similar scientific discipline; an associates degree is acceptable with at least 3 years of relevant industry experience.

• Minimum of 1 year of experience working in a GMP-regulated environment.

• Minimum of 1 year of industry laboratory experience, preferably in manufacturing, bioprocessing, or related life sciences operations.

• Demonstrated proficiency in aseptic and sterile technique, verified through references or prior work experience.

• Strong writing skills, including the ability to produce clear, accurate, and compliant documentation, verified by references.

• Hands-on experience with laboratory procedures such as reagent preparation, sample handling, and data recording.

• Ability to follow detailed SOPs, adhere to Good Documentation Practices (GDP), and maintain meticulous records.

• Capability to operate and maintain laboratory and manufacturing equipment used in cell processing, encapsulation, microscopy, and cell counting.

• Commitment to working within biosecurity requirements, including avoiding residence on or near swine farms and refraining from routine contact with swine.

Additional Skills & Qualifications

• Experience in FDA-regulated manufacturing environments.

• Cleanroom or controlled environment experience, including familiarity with gowning procedures and cleanroom protocols.

• Background in cell-based therapies, bioprocessing, or pharmaceutical manufacturing.

• Strong attention to detail and ability to identify and report deviations or nonconformances.

• Comfort working with production and laboratory data to support quality and process improvement.

• Interest in contributing to innovative therapies that have the potential to improve the lives of people with Type 1 diabetes.

• Motivation to grow within a company that promotes from within and offers opportunities for career development.

Work Environment

This role is based in a GMP-regulated cleanroom and controlled environment, requiring full sterile gowning and adherence to strict aseptic and biosecurity protocols. You will work in a new, biosecure research and manufacturing facility that is unmarked and designed with a discreet exterior similar to an airplane hangar. The standard schedule is Monday through Friday, approximately 6:30 a.m. to 4:00 p.m., with the potential for infrequent weekend shifts as operational needs arise. The environment emphasizes safety, regulatory compliance, and teamwork, and offers the opportunity to support clinical-stage manufacturing of a unique encapsulated product that aims to improve outcomes for individuals with Type 1 diabetes. The culture supports internal promotion, professional development, and collaboration in a high-growth setting transitioning from R&D to full-scale GMP manufacturing.

Job Type & Location

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

Application Deadline

This position is anticipated to close on Oct 22, 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 View email address on click.appcast.io 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.