GMP Quality Assurance Specialist - CDMO (Raleigh-Durham)

Meet Life Sciences Ltd.

North Carolina

On-site

USD 70,000 - 90,000

Full time

2 days ago

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Job summary

Meet Life Sciences Ltd. is seeking experienced Quality Assurance professionals for multiple opportunities in the Raleigh-Durham area.

Positions span QA Specialist, QA Associate, QA Compliance, batch record review, deviations, CAPA, change control, and document control in GMP-regulated pharmaceutical/biotech environments. Candidates with CDMO experience and strong quality systems knowledge are encouraged to apply, with roles potentially available across various experience levels and quality

Qualifications

Previous experience working in a GMP-regulated environment is required.
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.

Responsibilities

Quality roles include QA Specialist, QA Associate, QA Compliance.
Perform batch record reviews and deviations investigations.
Support CAPA, change control, and document control processes.
Ensure compliance with GMP and regulatory requirements in manufacturing environments.