In this role you will safeguard quality standards across the quality management system in a Biopharma setting. You will lead internal audits, drive CAPA with cross-functional teams, and ensure regulatory compliance. You will train colleagues on QA processes, sharing best practices. You will shape quality systems in a sterile environment and contribute to the company’s quality excellence journey.
Responsibilities
Oversee and maintain the quality management system to ensure compliance with industry standards
Conduct internal audits and inspections to identify areas for improvement
Collaborate with cross-functional teams to implement corrective and preventive actions
Provide training and guidance on quality assurance processes and best practices
Key requirements
Relevant degree in a scientific or technical discipline
Proven industry experience in quality assurance within a Sterile environment
Working knowledge and practical experience with quality management systems and regulatory requirements
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