The Role
Provide quality oversight for manufacturing, validation, facilities, and environmental programs to ensure GMP and regulatory compliance. Perform electronic batch record (EBR) review, approval, and reconciliation, oversee manufacturing operations, manage quality events, and support decision-making.
Summary Generated by Built In
We are seeking a QA Specialist to provide quality oversight for manufacturing operations, validation activities, facilities, and environmental programs, ensuring compliance with GMP standards and regulatory requirements.
Requirements
- Doctorate or Master’s + 2 years of Scientific experience; or Bachelors + 4 years of Scient
ific experience.
- Experience performing batch record (EBR) review, approval, and reconciliation.
- Oversight manufact
uring operations.
Manage events and decision making.
Skills Required
- Doctorate or Master's plus 2 years of scientific experience; or Bachelor's plus 4 years of scientific experience.
- Experience performing batch record (EBR) review, approval, and reconciliation.
- Oversight of manufacturing operations.
- Ability to manage events and support decision making.
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The Company
What We Do
QRC Group specializes in providing expert consulting services in regulatory compliance, quality management, and risk management for the pharmaceuticals, medical devices, biotechnology, and other regulated industries, delivering comprehensive project management and validation solutions.
