Quality Associate and Quality Control
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We are seeking experienced Quality Assurance professionals for multiple opportunities with established Contract Development and Manufacturing Organization (CDMO) clients in the Raleigh-Durham area.
If you have experience working in a GMP-regulated pharmaceutical, biotechnology, or life sciences environment, we encourage you to apply
Quality Assurance (QA)
Quality Specialist, QA Associate, QA Compliance, Batch Record Review, Deviations, CAPA, Change Control, and Document Control.
Qualifications
- Previous experience working in a GMP-regulated environment is required.
- Previous CDMO experience is highly preferred.
- Experience supporting pharmaceutical or biotechnology manufacturing, quality systems, or laboratory operations.
- Knowledge of applicable quality standards, documentation practices, and regulatory requirements.
- Strong attention to detail, organizational skills, and a commitment to product quality and compliance.
Why Apply?
Explore multiple opportunities with CDMO clients throughout the Raleigh-Durham area, with positions potentially available across different experience levels and quality functions.
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