Gevestigd apotheker Spits apotheek Alkmaar

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

• Ensure overall responsibility for pharmaceutical quality and compliance with applicable laws, regulations, and GDS standards
• Develop, maintain, and continuously improve the Quality Management System (QMS)
• Monitor and enforce adherence to procedures, policies, and regulatory requirements across the organization
• Act as the primary contact for quality-related issues, including customer complaints and regulatory inquiries
• Approve validation, calibration, and deblistering protocols, as well as procedural deviations and changes
• Oversee and ensure proper handling of deviations, CAPAs, and recalls
• Authorize release of packaging processes, validated equipment, and repackaged medication
• Lead and support internal and external audits and maintain relationships with regulatory bodies
• Provide leadership, coaching, and guidance to quality teams and broader organization
• Promote a strong quality culture and continuous improvement mindset across all functions
• Evaluate product changes, risks, and impacts related to pharmaceutical properties and packaging
• Has authority to stop production and block products in case of quality risks

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• Master’s Degree in Pharmacy
• Valid and unrestricted registration in the relevant professional register (e.g., BIG register or equivalent)
• Minimum 3 years of experience in a similar role within a regulated pharmaceutical environment
• Strong knowledge of pharmaceutical regulations, GDP and GMP guidelines
• Experience with Quality Management Systems and regulatory compliance frameworks
• Experience working with audits and regulatory inspections
• Proven experience in validation of equipment and software
• Strong leadership and people management experience, including coaching and development
• Experience in process improvement and organizational optimization
• Excellent communication and stakeholder management skills
• Strong analytical skills and ability to translate strategy into operational processes

• Strong leadership and team management capabilities
• Advanced knowledge of pharmaceutical quality standards and regulatory frameworks
• Decision-making skills, including ability to act in critical or urgent situations
• High attention to detail and problem-solving abilities
• Strong analytical and critical thinking skills
• Ability to influence and drive change within an organization
• Excellent communication and collaboration skills
• Organizational awareness and ability to navigate complex stakeholder environments
• Results-oriented mindset with focus on continuous improvement
• Fluency in English (written and spoken)

​Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.