Manufacturing Support Associate

The Manufacturing Support Associate plays a crucial role in maintaining GMP readiness of cleanrooms by performing routine and ad-hoc facility sanitization, conducting viable and non-viable environmental monitoring, and supporting the flow of materials, equipment, and products throughout the facility. This position is highly detail-oriented and documentation-driven, essential for contamination control and ensuring patient safety.

• Perform routine and ad-hoc cleaning of classified cleanrooms in accordance with SOPs, cGMP requirements, and regulatory expectations.
• Accurately complete cleaning logs and documentation to ensure GDP compliance.
• Support inspection readiness by maintaining cleanroom standards and promptly addressing deviations.
• Safely transfer raw materials, consumables, drug products, and equipment throughout the facility, including classified locations.
• Support material staging and preparation to enable timely manufacturing operations.
• Assist production staff with ancillary support tasks, such as cryopreservation transfer tasks.
• Adhere strictly to GMP, GDP, and safety requirements during all activities.
• Comply with all local policies and SOPs governing tasks performed.
• Maintain training status, including aseptic gowning qualification and requalification.
• Identify and escalate any deviations or anomalies observed during cleaning, environmental monitoring, or material handling.
• Participate in training, audits, and continuous improvement initiatives such as 5S/Kaizen to sustain a culture of quality and compliance.

• Associate's degree in the sciences.
• Strong documentation skills with GMP.
• Experience in biologics, aseptic techniques, microbiology, laboratory work, and biology.
• Environmental monitoring, aseptic technique, cleanroom gowning, GMP, and GDP.

• Bachelor’s degree in a science-based discipline (e.g., biology, chemistry, biotechnology) preferred.
• Prior experience with cleanroom sanitization, environmental monitoring execution, and/or materials handling is strongly preferred.
• Strong attention to detail with proven ability to follow SOPs and GDP requirements.
• Strong teamwork and communication skills with flexibility to support cross-functional needs.

This role is within a leading US-based cell therapy contract development and manufacturing organization specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical and commercial supply. The organization operates from two U.S.-based manufacturing facilities and combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of a global leader in the pharmaceutical and biotechnology sectors. The work involves being in cleanroom environments, requiring the use of PPE and adherence to rigorous safety standards.

This is a Contract to Hire position based out of Princeton, NJ.

The pay range for this position is $32.00 - $32.00/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 Princeton,NJ.

This position is anticipated to close on Dec 19, 2025.

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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $32