Quality Control PCR specialist - 157895

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 currently looking for an experienced Quality Control PCR Specialist in Exton, Pennsylvania (PA) to work for a pharmaceutical cell therapy company.

Responsibilities for the Quality Control PCR Specialist include:

• Utilize skills with PCR, HPLC (Empower), SDS-Page, Elisa, Gel Electrophoresis, and UV-VIS to assist in the production of cell therapy products
• Support process Improvement projects such as standardization of test methods and the execution of test methods as well as assay validation/ qualification
• Perform OOS/ Deviation investigations and carry our experiments in support of these investigations
• Ensure compliance with regulations, guidelines and procedures

Qualifications for the Quality Control PCR Specialist include:

• 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
• Bachelor’s degree in chemistry or related field

Compensation for the Quality Control PCR Specialist include:

• Compensation is $40.00/hr
• Comprehensive benefits package

Keywords

Pharmaceutical, quality control, PCR, Elisa, SDS Page UV-Vis, Deviation, OOS, Investigations, Assay qualification, technical writing, FDA, manufacturing, Science, comprehensive benefits package, Health, Vision, Dental #LI-ONSITE #LI-DF1