Quality Control Specialist

Piper Companies; Branchburg Township (NJ); On-site; USD 55,104 - 66,124; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

A pharmaceutical cell therapy company in Branchburg, New Jersey, is seeking an experienced Quality Control Specialist. The successful candidate will have a minimum of 4 years of experience in quality control, hands-on expertise in Flow Cytometry and PCR testing, and the ability to conduct investigations for deviations or out-of-specifications. This role offers a competitive hourly rate of $40-$48 along with a comprehensive benefits package.

Qualifications

• Minimum of 4+ years’ experience within quality control.
• Hands-on experience conducting Flow Cytometry and PCR testing.
• Ability to conduct deviation or OOS investigations.
• Experience within cell therapy or biologics manufacturing.

Responsibilities

• Perform analytical testing under cGMP in collaboration with QC.
• Utilize knowledge of aseptic techniques using a BSC.
• Track and trend analytical methods and assist in troubleshooting.
• Document testing in accordance with cGMP requirements.

Skills

Flow Cytometry

PCR Testing

Analytical Testing

Technical Writing

Education

Bachelor's degree in chemistry or related field

Job description

Overview

Piper Companies is currently looking for an experienced Quality Control Specialist in Branchburg, New Jersey (NJ) to work for a pharmaceutical cell therapy company. Must have experience with Flow Cytometry experience.

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

Qualifications

• A minimum of 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
• Hands on experience within cell therapy or biologics manufacturing
• Technical writing experience preferred
• Bachelor’s degree in chemistry or related field

Compensation

• Compensation is $40.00/hr - $48.00/hr
• Comprehensive benefits package

Keywords

Pharmaceutical, quality control, Analytical Chemistry, Cell Therapy, Biologics, PCR, Flow Cytometry, Deviation, OOS, Investigations, Assay qualification, technical writing, FDA, manufacturing, Science, comprehensive benefits package, Health, Vision, Dental