Cell Therapy Manufacturing Technician

ClinLab Solutions Group; New Jersey; On-site; USD 75,000 - 105,000; Full time

Job summary

ClinLab Solutions Group in New Jersey is seeking a detail-oriented professional to support cell therapy production in a regulated cleanroom environment, emphasizing aseptic technique and quality standards. You will perform aseptic manufacturing, handle cell culture, formulation, cryopreservation, and document processes with strict traceability to regulatory requirements.

The role requires teamwork, adaptability, and the ability to operate specialized equipment in a fast-paced setting while

Qualifications

• Bachelor’s degree in Biology, Biotechnology, or related field (or equivalent experience).
• 1–3 years in GMP manufacturing, preferably cell therapy or biologics.
• Strong aseptic technique and cleanroom operations knowledge.
• Detail-oriented with strong quality focus.
• Able to follow batch records and regulatory guidelines.

Responsibilities

• Perform aseptic manufacturing operations in a cleanroom per cGMP and safety protocols.
• Execute cell therapy manufacturing procedures, including culture, formulation, and cryopreservation.
• Operate and maintain specialized manufacturing equipment.
• Document production processes with traceability and regulatory compliance.
• Support investigations of deviations and change controls with cross-functional teams.
• Participate in training, audits, validation, and SOP/batch record reviews.

Skills

Aseptic technique

Attention to detail

Quality systems

Team collaboration

Adaptability

Documentation

Education

Bachelor’s degree in Biology/ Biotechnology or related field

Tools

5S principles

Microsoft Office

Electronic batch records

Job description

ClinLab Solutions Group in New Jersey is seeking a detail-oriented professional to support cell therapy production in a regulated cleanroom environment, emphasizing aseptic technique and quality standards. You will perform aseptic manufacturing, handle cell culture, formulation, cryopreservation, and document processes with strict traceability to regulatory requirements.

The role requires teamwork, adaptability, and the ability to operate specialized equipment in a fast-paced setting while