Manufacturing Support Technician
Actalent
Posted Thursday, May 7, 2026
Posting ID: JP-006010835
Job Description
The Manufacturing Support Technician participates in the complex manufacturing of modern, cutting-edge cell therapy products in a cGMP-compliant cleanroom environment. This role supports the production of RNA cell therapies and other biologics by maintaining manufacturing areas, handling GMP materials, and ensuring strict adherence to regulatory and safety standards. The position is ideal for individuals who are passionate about advanced cell therapy, committed to high-quality documentation, and eager to contribute to transformative treatments for patients with autoimmune diseases.
Responsibilities
- Maintain manufacturing facilities by transferring GMP materials into the cleanroom suites, following all aseptic and gowning requirements.
- Adhere strictly to Standard Operating Procedures (SOPs) and accurately document all activities in accordance with cGMP requirements.
- Maintain a clean, organized, and compliant manufacturing space, ensuring adherence to all safety and regulatory guidelines.
- Clean, operate, and maintain the Process Waste area, ensuring the area remains orderly and free of unnecessary materials.
- Discard waste materials within the Process Waste area and clean drums, dollies, and related equipment as required.
- Stock and replenish general supplies in the manufacturing production areas to support continuous operations.
- Handle and discard hazardous and non-hazardous waste in accordance with established procedures and safety standards.
- Perform routine equipment cleaning and basic upkeep as needed to support reliable manufacturing operations.
- Support the setup and operation of complex equipment in a cleanroom environment as part of the manufacturing process.
- Apply attention to detail and follow good documentation practices when recording data and completing manufacturing records.
- Collaborate with internal teams and communicate effectively to support smooth production workflows.
- Perform other duties as assigned to support biologics and cell therapy manufacturing activities.
- 1+ years of experience in manufacturing or biopharmaceutical processing in a cGMP environment with a Bachelor’s degree, or 3+ years of experience in manufacturing or biopharmaceutical processing in a cGMP environment with a high school diploma.
- Experience working in a cGMP production environment for biologics, with cell therapy experience strongly preferred.
- Significant knowledge of biologics manufacturing processes, cell culture, and/or cell therapy production.
- Demonstrated experience working in a cleanroom environment with strict aseptic techniques.
- Proficiency with aseptic processing and gowning procedures required for cleanroom operations.
- Strong documentation skills, including the ability to follow and complete documentation associated with cGMP manufacturing.
- Ability to apply critical thinking and independent decision-making to complex biologics and cell therapy manufacturing processes.
- High attention to detail and strong troubleshooting skills in a regulated manufacturing setting.
- Proficient communication abilities to interact effectively with internal teams.
- Ability to stand for extended periods (3–6 hours at a time) and lift up to 30 pounds while performing manufacturing and support tasks.
- BS degree in Life Sciences or Engineering is highly valued for this role.
- Prior hands-on experience in cell therapy or biologics manufacturing is preferred.
- Familiarity with RNA cell therapy concepts and processes is beneficial.
- Comfort working with biological materials in a controlled cleanroom environment.
- Ability to work occasional weekends and holidays as needed to support manufacturing schedules.
- Strong sense of responsibility for safety, environmental, and health considerations in the workplace.
- Motivation to contribute to pioneering therapies for patients with autoimmune diseases, including products in late-stage clinical development.
This position is based in a modern manufacturing facility with a strong focus on advanced cell therapy and biologics production. The role requires hands-on work setting up and operating complex equipment in a cGMP-compliant cleanroom environment. The work setting places continuous emphasis on safety, environmental, and health considerations, and requires strict adherence to all company policies, rules, and regulations. Daily activities involve handling biological materials in a cleanroom, where appropriate personal protective equipment is required, including eye protection, mask, coverall gown, gloves, and shoe covers. Team members spend extended periods standing in the cleanroom, typically 3–6 hours at a time, and must be able to lift up to 30 pounds. The standard schedule is Monday through Friday from 8:30 a.m. to 5:00 p.m., with the possibility of occasional weekend work, approximately once per month and generally on a volunteer basis, as well as occasional holiday work to support production needs. The environment is collaborative and mission-driven, centered on reimagining cell therapies with transformative technologies to bring a new generation of treatment options to patients with autoimmune diseases.
Job Type & Location
This is a Contract position based out of Frederick, MD.
Pay and BenefitsThe pay range for this position is $27.00 - $30.00/hr.
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)
This is a fully onsite position in Frederick,MD.
Application DeadlineThis position is anticipated to close on May 20, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 actalentaccommodation@actalentservices.com 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.
Contact Information
Recruiter: Alexis Atkinson
Phone: +14105678051
Email: alatkinson@actalentservices.com
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