Associate, QC Analytical, Cell TherapyWed-Sat 1:30-11:30

Spectraforce Technologies; Summit (NJ); On-site; USD 34,440 - 55,104; Full time

Job summary

Spectraforce Technologies is seeking an Associate, QC Analytical in Summit, NJ, for a 6‑month assignment. The role supports QC testing for in‑process, final product, and stability samples, with responsibilities including documentation, deviations, investigations, and improvements.

The ideal candidate has a science degree (BS preferred or assoc. with commensurate experience) and 0–2+ years in analytical QC, with lab skills in basic techniques and aseptic handling.

Qualifications

• Bachelor's degree in science preferred; associate's degree with equivalent experience may be considered.
• 0–2+ years of relevant 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.
• 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

Analytical testing

Cell biology techniques

qPCR

Flow cytometry

Aseptic technique

Documentation & CAPA

Education

Bachelor's degree in science

Associate's degree with equivalent experience

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 1:30-11:30

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.