Quality Control PCR Specialist — GMP Lab, Cell Therapy

Piper Companies; Exton (PA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Comprehensive benefits package

Hourly pay $40

Job summary

Piper Companies is seeking a Quality Control PCR Specialist in Exton, Pennsylvania (PA) to support a pharmaceutical cell therapy company. The role requires a minimum of 2 years in QC and hands-on PCR testing in a GMP lab, with responsibilities including deviation investigations and ensuring regulatory compliance.

The position offers $40.00/hr with a comprehensive benefits package. On-site work in Exton, PA, with opportunities to contribute to assay qualification and method standardization.

Qualifications

• A minimum of 2 years’ experience within quality control.
• Hands on experience conducting PCR testing within a GMP laboratory environment.
• Ability to conduct a deviation or OOS investigation.
• Technical writing experience preferred.

Responsibilities

• Utilize PCR, HPLC (Empower), SDS-PAGE, ELISA, Gel Electrophoresis, and UV-Vis to assist in production of cell therapy products.
• Support process improvement projects including standardization of test methods and assay qualification/validation.
• Perform OOS/Deviation investigations and carry out experiments in support of these investigations.
• Ensure compliance with regulations, guidelines and procedures.

Skills

PCR testing

HPLC

SDS-PAGE

ELISA

Gel electrophoresis

UV-Vis

Deviation investigations

Technical writing

GMP compliance

Education

Bachelor's degree in chemistry

Tools

Empower

PCR instrumentation

Job description

Piper Companies is seeking a Quality Control PCR Specialist in Exton, Pennsylvania (PA) to support a pharmaceutical cell therapy company. The role requires a minimum of 2 years in QC and hands-on PCR testing in a GMP lab, with responsibilities including deviation investigations and ensuring regulatory compliance.

The position offers $40.00/hr with a comprehensive benefits package. On-site work in Exton, PA, with opportunities to contribute to assay qualification and method standardization.