Associate, QC Analytical, Cell Therapy
•2 days ago
| Hours | Full-time, Part-time |
|---|---|
| Location | Summit, New Jersey |
About this job
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: Sunday - Wednesday 1:30pm-11:30pm
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.
Location: Summit West, NJ, 07901
Duration: 06 Months
Reporting relation: This position will report to QC management.
Shift: Sunday - Wednesday 1:30pm-11:30pm
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.
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