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

Spectraforce Technologies, Inc.; Summit (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

Spectraforce Technologies, Inc. seeks an Associate, QC Analytical, Cell Therapy to support quality control testing in Summit, NJ.

This 6-month role focuses on in-process, final product, and stability samples and may involve documentation and investigations. The ideal candidate has 0-2+ years in analytical testing within a regulated environment, familiarity with cell biology techniques such as flow cytometry and qPCR, and a solid grasp of GMP practices.

Qualifications

• Bachelor's degree preferred in science or an equivalent combination of education and experience.
• 0-2+ years of relevant analytical testing or QC experience, preferably in a regulated environment.
• Familiarity with basic laboratory techniques and safety practices.

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-related tasks and continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Skills

QC testing

GMP documentation

Data verification

Team communication

Attention to detail

Education

Bachelor's degree preferred in science

Associate's degree with equivalent education/experience

Tools

Cell-based assays

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 - Sun - Wed - 1:30 PM - 11:30 PM

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.