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
US$20 - US$24 per hour + Highly Competitive Salary
Hoover, USA
Ready to grow your career in sterile compounding? Looking to join a thriving pharmaceutical operation and help deliver exceptional standards of quality and compliance.
Highly Competitive
Philadelphia, USA
Play a crucial role in advancing life-changing cell and gene therapies by ensuring GMP production environments remain audit-ready and contamination-free.
Highly Competitive
Aargau, Switzerland
Be the driving force behind seamless logistics for a global CMO, where precision and efficiency for quality are key to supporting world-class manufacturing.
Highly Competitive
Bristol, USA
Join a team transforming the future of medicine through cutting-edge bioconjugation and gene therapy manufacturing.
Highly Competitive
Bern, Switzerland
Do you thrive on solving complex quality challenges and turning investigations into lasting improvements?
Highly Competitive
Mansfield, USA
Join a team where precision, quality, and scientific excellence come together to help deliver safe and effective pharmaceutical products.
Highly Competitive
Norton, USA
Passionate about quality and compliance? Join a team where your expertise helps ensure every biopharmaceutical product meets the highest standards of safety and excellence.
Highly Competitive
Paris, France
Notre client recherche un Coordinateur QHSE Prestataires pour rejoindre leur équipe et intervenir sur le site de l'un de leurs clients majeurs en pharmaceutique.
Highly Competitive
Hatfield, England
Lead the quality agenda, shape compliance excellence, and make a lasting impact on the delivery of safe, high-quality pharmaceutical products.