Specialist QA36
- Contract
Company Description
QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!
Job Description
- Strong knowledge of and experience with processes involved in manufacturing, QA, QC, validation and process development.
- Demonstrate ability to interact with regulatory agencies
- Review and approve product MPs.
- Approve process validation protocols and reports for manufacturing processes.
- Approve Environmental Characterization reports.
- Lead investigations and site audits.
- Review Risk Assessments.
- Approve NC investigations and CAPA records.
- Approve change controls.
- Provide lot disposition and authorize lots for shipment.
- Non-Standard 2nd and 3rd shifts
Qualifications
- Doctor OR Master’s degree in Life Science or Engineering and 3 years of Manufacturing or Quality in GMP regulated environment experience
OR
- Bachelor’s degree in Life Science or Engineering and 5 years of Manufacturing or Quality in GMP regulated environment experience.
Additional Information
Send resume preferable in Word format
Willing to work as Independent Consultant
Non-Standard 2nd and 3rd shifts