Quality Control Specialist - Flow Cytometry & Cell Therapy

ZP Group; Branchburg Township (NJ); On-site; USD 55,000 - 66,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking a Quality Control Specialist in Branchburg, New Jersey to join a pharmaceutical cell therapy company. The ideal candidate has 4+ years of quality control experience and hands-on Flow Cytometry and PCR testing in a GMP setting.

Responsibilities include analytical testing, aseptic technique using a BSC, trend analysis, equipment maintenance, and documentation of testing in accordance with cGMP requirements; OOS/Deviations investigations are part of the role.

Qualifications

• 4+ years’ experience within quality control.
• Hands-on experience conducting Flow Cytometry and PCR testing within a GMP laboratory environment.
• Ability to conduct a deviation or OOS investigation; technical writing preferred.

Responsibilities

• Perform analytical testing (cell-based function, flow cytometry, and PCR-based assays) under cGMP in collaboration with QC.
• Utilize knowledge of aseptic techniques using a BSC.
• Track and trend analytical methods and assist in troubleshooting activities.
• Maintain, calibrate, and operate analytical equipment.
• Maintain laboratory material and reagent inventory.
• Document testing in accordance with cGMP requirements.
• Perform OOS/Deviation investigations and carry out experiments in support of these investigations.

Education

Bachelor’s degree in chemistry or related field

Tools

Flow Cytometry

PCR testing

GMP laboratory practices

Job description

Piper Companies is seeking a Quality Control Specialist in Branchburg, New Jersey to join a pharmaceutical cell therapy company. The ideal candidate has 4+ years of quality control experience and hands-on Flow Cytometry and PCR testing in a GMP setting.

Responsibilities include analytical testing, aseptic technique using a BSC, trend analysis, equipment maintenance, and documentation of testing in accordance with cGMP requirements; OOS/Deviations investigations are part of the role.