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Senior Quality Director

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Job Title: Director of Quality (Qualified Person) – Sterile Manufacturing Site
Location: We are seeking a highly experienced and strategic Director of Quality to lead the quality operations at our sterile manufacturing site located in the South of France. As the Director of Quality, you will oversee a team of approximately 50 professionals and ensure compliance with all relevant regulations, standards, and guidelines to maintain the highest quality of sterile products.

Quality Leadership: Provide strategic direction and leadership to the Quality Department, ensuring alignment with company objectives and industry best practices.
Ensure all products meet safety, quality, and efficacy standards.
Manage and mentor a team of approximately 50 quality professionals, including Quality Assurance (QA), Quality Control (QC), and Quality Systems teams.
Drive a culture of continuous improvement by implementing best practices, identifying process improvements, and managing quality risk assessments.
Cross-Functional Collaboration: Collaborate with Manufacturing, R&D, Supply Chain, and other departments to ensure quality is integrated into all aspects of production and product development.
Strategic Planning: Develop and execute a strategic quality plan that supports the overall business strategy, focusing on growth, efficiency, and sustainability of sterile manufacturing operations.
Performance Management: Set performance goals, conduct regular reviews, and implement training programs to ensure the team remains highly skilled and motivated.
Lead investigations into product quality issues, non-conformances, and deviations, ensuring effective root cause analysis and corrective and preventive actions (CAPAs).
Serve as the primary point of contact for quality-related matters with internal and external stakeholders, including customers, regulatory authorities, and suppliers.

Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related scientific discipline; a Master's or Doctorate is preferred.
Minimum of 10 years of experience in quality management within a sterile pharmaceutical or biopharmaceutical manufacturing environment.
Proven track record in a senior leadership role, managing large teams and implementing strategic initiatives.
Fluent in English and French (preferred).

Ability to drive a culture of quality and continuous improvement across the organization.

Competitive salary and performance-based bonuses.
Relocation assistance for the right candidate.
Opportunities for professional development and career progression.