Similar posts
QA Specialist
- Permanent
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a QA Specialist with a biotechnology company located in Marietta, PA. The candidate will ensure all cGMPs, validation, quality, safety and environmental regulations are met and adhere to all safety guidelines and procedures.
Job Responsibilities:
- Perform technical review of cGMP documentation and Batch Records for completeness and compliance to cGMPs as outlined by governmental regulations and internal procedures
- Provide advice and counsel on cGMP and related quality assurance issues to the value stream
- Demonstrate sound decision making relating to quality issues
- Provide on the floor QA support and perform QA Operations activities
- Take initiative to resolve quality documentation concerns
- Perform review and support regarding discrepancies and/or anomalies noted during QA review of associated processes
- React to and escalate production issues
- Routinely communicate and report deviations from procedures/processes to Quality Assurance Management and initiate appropriate action as necessary
- Write and/or revise controlled documents in support of job responsibilities
Skills and Requirements:
- BS/BA in biology, chemical engineering, life sciences. Degree in other discipline if sufficient technical depth has been achieved from professional experience
- QA experience preferred. Minimum 1 year also preferred.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Zachary Hines at 215-531-6914 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-ZH1
#Compliance/Quality
Related jobs
Highly Competitive
Visp, Switzerland
Join a leading Swiss team as a QC Associate driving excellence in biopharmaceutical quality control.
Highly Competitive
Rockville, USA
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Highly Competitive
Liverpool, England
Are you passionate about quality and precision? Join our client in this Quality Assurance Representative and help ensure top-tier standards every day.
Highly Competitive
Bristol, USA
Drive cGMP excellence by powering large‑scale downstream manufacturing that brings life‑changing therapies to reality.