Job Title: Manufacturing Support TechnicianJob 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.
Essential Skills
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.
Additional Skills & Qualifications
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.
Work Environment
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 Benefits
The 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)
Workplace Type
This is a fully onsite position in Frederick,MD.
Application Deadline
This position is anticipated to close on May 18, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC-with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.
