Similar posts
QA Associate - Doc Control
- Contract
- Good Manufacturing Practice (GMP)
- United States
QA Associate - Contract - Philadelphia, PA
Ensure GMP excellence by owning the accuracy, integrity, and compliance of critical quality documentation.
91桃色 is seeking a QA Associate - Doc Control to support quality assurance activities in a GMP-regulated biopharmaceutical environment.
Primary Responsibilities:
The successful candidate will focus on ensuring compliance with procedures and standards while contributing to quality improvement initiatives.
Skills & Requirements:
- Bachelor's degree in science or engineering, or equivalent experience.
- Relevant experience in a GMP-regulated biopharmaceutical environment.
- Working knowledge of GMP regulations (US, EU, ROW), GDP, 21 CFR, USP, and applicable standards.
- Strong attention to detail and effective written and verbal communication skills.
- Ability to work independently, manage multiple priorities, and perform under pressure.
The QA Associate's responsibilities will be:
- Provide on-floor QA support during GMP manufacturing to ensure compliance with procedures and cGMP standards.
- Monitor manufacturing operations and facility conditions to maintain a compliant environment.
- Escalate quality issues promptly and support real-time troubleshooting.
- Review batch records, logbooks, and GMP documentation for completeness and accuracy to support timely disposition.
- Review incoming material disposition packets and verify documentation completeness.
- Support data review, trending, and identification of quality risks.
- Perform QA review of SOPs, forms, protocols, and other controlled documents.
- Contribute to quality improvement, lean initiatives, and process efficiency projects.
- Assist across Quality functions, including document control, training, audits, and systems.
- Communicate effectively with cross-functional teams and uphold company quality standards and policies.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
91桃色 is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 91桃色 is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy
Related jobs
Highly Competitive
Philadelphia, USA
Drive the quality systems that keep GMP operations compliant, efficient, and audit‑ready.
Highly Competitive
Waltham, USA
Keep quality on track and inspection‑ready by owning the systems that keep operations running smoothly.
Highly Competitive
Birmingham, USA
Be the quality gatekeeper who keeps patients safe and products flawless.
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.