Associate, QC Analytical, Cell TherapyWed-Sat 6:30-4:30

Spectraforce Technologies; Summit (NJ); On-site; USD 55,000 - 75,000; Full time

Job summary

Spectraforce Technologies is hiring for an Associate, QC Analytical, Cell Therapy in Summit, NJ. The role focuses on supporting routine QC testing across in-process, final product, and stability samples, with opportunities to assist with documentation, deviations, investigations, and continuous improvement initiatives.

The position requires 0–2+ years of relevant QC experience, basic lab techniques, and knowledge of cell/molecular biology methods.

Qualifications

• Bachelor's degree preferred in science; associate degree with equivalent experience also considered.
• 0–2+ years of analytical testing or QC experience in a regulated environment.
• Demonstrated experience with basic lab techniques and lab safety practices.
• Experience with cell and molecular biology techniques (cell-based assays, flow cytometry, qPCR) preferred.

Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, CAPA, deviation/investigation tasks and continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Skills

Procedural adherence

Lab techniques

Communication

Attention to detail

Teamwork

Education

Bachelor's degree preferred in science

Associate's degree with equivalent education/experience

0–2+ years analytical testing/QC experience

Cell/Molecular biology techniques knowledge

Laboratory safety practices

Job description

Position Title

Associate, QC Analytical, Cell Therapy

Location

Summit West, NJ, 07901

Duration

06 Months

Reporting Relation

This position will report to QC management.

Shift

Associate, QC Analytical, Cell Therapy Wed-Sat 6:30-4:30

Purpose and Scope of Position

Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.

Duties / Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, project, CAPA, deviation/investigation-related tasks and/ or continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Specific Knowledge, Skills, Abilities

• Ability to accurately and completely understand and follow procedures.
• Apply scientific principles to analytical testing and the proper use of laboratory equipment.
• Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
• Attention to detail and demonstrated organizational skills.
• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Education / Experience / Licenses / Certifications

• Bachelor's degree preferred in science. Associate's degree with equivalent combination of education and work experience may be considered.
• 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
• Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.