Senior Quality Manager – R&D

• Ensure quality oversight for complex R&D projects and global quality initiatives
• Act as the key QA partner for cross-functional stakeholders and project teams
• Review, approve, and release GMP-relevant documentation and quality deliverables
• Drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives
• Support validation, qualification, and continuous improvement projects
• Provide expert guidance on cGMP compliance and quality standards
• Contribute to audits, inspections, and due diligence activities
• Promote operational excellence and a strong quality culture across the organization

• Bachelor's degree with 5+ years of experience or Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations
• Strong knowledge of cGMP regulations, quality systems, and regulatory requirements
• Experience in quality risk management, deviations, change controls, and CAPA processes
• Strong project management, stakeholder management, and decision-making skills
• Solid scientific, technical, and compliance knowledge within the pharmaceutical industry
• Fluent in English
• Nice to have: Experience with validation, analytical development, health authority inspections, and global project environments

• Talent Management – We support your professional growth and help you develop your career.
• Work-Life Balance – Flexible working hours and the opportunity for mobile working.
• Green Mobility – Benefit from our public transportation subsidy and enjoy discounted commuting.