À±½·ÊÓÆµ

QA Associate - Doc Control

Highly Competitive
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. United States
Philadelphia, USA
Posting date: 30 Mar 2026
69075

QA Associate - Contract - Philadelphia, PA

Ensure GMP excellence by owning the accuracy, integrity, and compliance of critical quality documentation.

À±½·ÊÓÆµ 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.

À±½·ÊÓÆµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓÆµ is acting as an Employment Agency in relation to this vacancy.

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