GMP Quality Systems Lead – Biopharmaceutical Manufacturing

Key Responsibilities

• Oversee quality control activities to ensure product compliance and quality standards.
• Support inspections and audits, ensuring adherence to GMP and regulatory requirements.
• Review documentation, investigate nonconformances, and lead CAPA initiatives.
• Drive continuous improvement projects to enhance quality processes.
• Collaborate with cross-functional teams to provide quality guidance and support training efforts.
• Maintain a culture of safety, compliance, and operational excellence aligned with patient-focused solutions worldwide.

Qualifications & Skills

• Strong understanding of GMP, regulatory standards, and quality systems.
• Experience in quality control, audits, and investigations.
• Excellent collaboration, communication, and problem-solving skills.
• Ability to support continuous improvement and foster a quality-focused environment.