Quality Control Specialist - 161288

Zachary Piper Solutions; Branchburg Township (NJ); On-site; USD 55,000 - 66,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies in Branchburg, New Jersey is seeking an experienced Quality Control Specialist to join our pharmaceutical cell therapy team onsite. The role emphasizes flow cytometry and PCR testing within a GMP environment, with responsibilities spanning analytical testing, aseptic technique, equipment upkeep, and investigation of deviations.

Qualified candidates have 4+ years in QC, hands-on flow cytometry and PCR in GMP labs, and a background in cell therapy or biologics manufacturing.

Qualifications

• 4+ years’ experience within quality control.
• Hands-on Flow Cytometry and PCR testing in a GMP lab.
• Ability to conduct a deviation or OOS investigation.
• Experience in cell therapy or biologics manufacturing.
• Technical writing experience preferred.
• Bachelor’s degree in chemistry or related field.

Responsibilities

• Perform analytical testing (cell-based function, flow cytometry, PCR-based assays) under cGMP with QC collaboration.
• Utilize aseptic techniques using a BSC.
• Track and trend analytical methods and assist in troubleshooting.
• 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 related experiments.

Skills

Flow Cytometry

PCR testing

Deviation investigations

GMP laboratory experience

Cell therapy/biologics exposure

Technical writing

Education

Bachelor’s degree in chemistry or related field

Job description

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 for the Quality Control Specialist include:

• 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 for the Quality Control Specialist include:

• 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 for the Quality Control Specialist include:

• 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 #LI-ONSITE #LI-DF1