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Manufacturing Associate

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Made Scientific
Full Time position
Listed on 2026-02-16
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Overview

Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Operating from two U.S.

-based manufacturing facilities, Made Scientific combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of GC Corporation of South Korea, a global leader in the pharmaceutical and biotechnology sectors.

Position Summary

The Manufacturing Associate will support Cell Therapy Operations at our GMP-compliant facility, playing a critical role in the production of cutting-edge cell therapies. This position is ideal for a detail-oriented professional with strong aseptic technique and a proven ability to quickly master complex processes in a cleanroom environment. The successful candidate will demonstrate a deep commitment to current Good Manufacturing Practices (cGMP) and thrive in a collaborative, quality-driven setting.

This role requires precision, adaptability, and a strong quality mindset to ensure the consistent delivery of high-standard therapeutic products.

Key Responsibilities
  • Perform aseptic manufacturing operations within a classified cleanroom environment, ensuring compliance with all cGMP and safety standards.
  • Execute complex procedures for cell therapy manufacturing and sterile product operations—including cell culture, formulation, and cryopreservation—while maintaining strict adherence to written procedures, batch records, and cGMP regulations.
  • Operate and maintain specialized manufacturing equipment, ensuring proper calibration and functionality.
  • Monitor and document all production processes with precision, ensuring traceability and compliance with regulatory standards.
  • Identify and escalate deviations or non-conformances; participate in root cause analyses and implement corrective actions.
  • Collaborate cross-functionally with Quality, Process Development, and Engineering teams to support continuous improvement initiatives.
  • Perform routine cleanroom maintenance, including environmental monitoring, cleaning, and sterilization activities.
  • Maintain an organized, compliant workspace by following 5S principles and minimizing contamination risks.
  • Participate in training sessions to stay current with manufacturing techniques, quality standards, and safety protocols.
  • Support process development activities during technology transfer.
  • Aseptically gown and work in ISO 8, 7, and 5 cleanroom environments and stand for extended periods.
  • Assist in creating and reviewing Standard Operating Procedures (SOPs) and Master Batch Records (MBRs).
  • Review MBRs daily to ensure documentation is accurate and complete.
  • Participate in audits, inspections, qualifications, and validation activities.
  • Handle chemicals such as corrosives, solvents, and biohazardous materials safely.
  • Perform other duties as assigned.
Required Qualifications
  • Bachelor’s degree in Biology, Biotechnology, or a related field preferred; equivalent experience will be considered.
  • 1–3 years of experience in GMP manufacturing, preferably in cell therapy, biologics, or pharmaceutical CDMO operations.
  • Strong knowledge of aseptic techniques and cleanroom protocols.
  • Proficiency in basic mathematical concepts, including scientific notation.
  • Proven ability to learn and master complex processes quickly.
  • Exceptional attention to detail with a strong commitment to quality standards.
  • Excellent collaboration, communication, and interpersonal skills.
  • Ability to work effectively in a fast-paced, dynamic environment with shifting priorities.
Preferred Qualifications
  • Experience in aseptic cell culture processing in ISO 5 biosafety cabinets, using universal precautions for handling human-derived materials.
  • Familiarity with cell therapy automation technologies, closed system culture vessels, cell washers, and cell separation technologies for autologous or allogeneic product manipulation.
  • Experience handling, propagating, isolating, activating, and cryopreserving human primary cells, including T cells.
  • Proficiency in basic computer applications (e.g.,…
Position Requirements
10+ Years work experience
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