Associate, QC Analytical, Cell TherapySun-Wed 1:30-11:30

Spectraforce Technologies; Summit (NJ); On-site; USD 60,000 - 86,000; Full time

Job summary

Spectraforce Technologies is seeking an Associate, QC Analytical, Cell Therapy in Summit, NJ for a 6-month assignment. The role supports QC testing of in-process, final product, and stability samples and reports to QC management.

You will perform routine testing, review GMP documentation, and assist with deviations, investigations, CAPA, and continuous improvement. Occasional training of analysts may be required; no remote work.

Qualifications

• Bachelor's degree preferred in science; Associate's degree with related experience may be considered.
• 0–2+ years of analytical testing or QC 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.

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.

Skills

Procedures compliance

Analytical testing

Lab equipment usage

Communication

Attention to detail

Team collaboration

Education

Bachelor's degree in science (preferred)

Associate's degree with related experience

0–2+ years QC experience

Basic lab techniques & safety

Cell/molecular biology techniques preferred

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: Sun-Wed 1:30-11:30 (Associate, QC Analytical, Cell Therapy)

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 an 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.