Associate, QC Analytical, Cell Therapy

Spectraforce Technologies, Inc.; Summit (NJ); On-site; USD 52,000 - 78,000; Part time

Job summary

Spectraforce Technologies, Inc. in Summit, NJ is seeking an Associate, QC Analytical, Cell Therapy to support in-process, final product, and stability testing. This role involves documentation review, deviations, investigations, and continuous improvement tasks in a GMP environment.

Ideal candidates have 0-2+ years of relevant QC experience or an equivalent education combination, with familiarity in basic lab techniques and cell/molecular biology methods such as flow cytometry or qPCR.

Qualifications

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

Responsibilities

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

Skills

Procedures adherence

Scientific testing principles

Laboratory equipment use

Effective communication

Detail oriented

Education

Bachelor's degree in science

Associate's degree with relevant experience

Tools

Flow cytometry

qPCR

Aseptic technique

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 7:00-5:00

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.