Manufacturing Support Associate

Job Title: Manufacturing Support AssociateJob Description The Manufacturing Support Associate is responsible for maintaining GMP readiness of cleanrooms through routine and ad-hoc sanitization, environmental monitoring, and supporting material and equipment flow within the facility. The role demands a high level of attention to detail and documentation, ensuring contamination control and patient safety. Responsibilities + Perform routine scheduled and ad-hoc cleaning of classified cleanrooms following SOPs and cGMP requirements. + Complete cleaning logs and documentation accurately to ensure GDP compliance. + Maintain cleanroom standards and address deviations promptly to support inspection readiness. + Safely transfer raw materials, consumables, drug products, and equipment throughout the facility, including classified locations. + Support material staging and preparation for timely manufacturing operations. + Assist production staff with ancillary support tasks, such as cryopreservation transfer tasks. + Adhere to GMP, GDP, and safety requirements during all activities. + Comply with local policies and SOPs governing tasks performed. + Maintain training status, including aseptic gowning qualification and requalification. + Identify and escalate deviations or anomalies observed during cleaning, environmental monitoring, or material handling. + Participate in training, audits, and continuous improvement initiatives like 5S/Kaizen. Essential Skills + GMP compliance + Environmental monitoring + Aseptic technique + Cleanroom gowning + Material management + Supply chain understanding + Excel proficiency, including Vlookups + Relevant pharmaceutical experience Additional Skills & Qualifications + Bacheloru2019s degree in a science-based discipline such as biology, chemistry, or biotechnology. + Experience in a GMP-regulated pharmaceutical, biotech, or CDMO environment. + Prior experience with cleanroom sanitization, environmental monitoring, and materials handling. Work Environment This position is within a leading US-based cell therapy contract development and manufacturing organization specializing in autologous and allogeneic cell therapy products. The organization operates from two U.S.-based facilities, combining the agility of a specialist CDMO with the expertise of a global leader in the pharmaceutical and biotechnology sectors. Job Type & Location This is a Contract to Hire position based out of Princeton, NJ. Pay and Benefits The pay range for this position is $30.00 - $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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Princeton,NJ. Application Deadline This position is anticipated to close on Feb 16, 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 due to a disability, please email ( ) for other accommodation options.

Created: 2026-02-04