Senior Quality Manager – R&D
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Job Description
Senior Quality Manager overseeing cGMP quality for pharmaceutical R&D projects at ALTEN, a global engineering services provider. Driving QA, risk management, documentation, and compliance initiatives.
Responsibilities:
- 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
Requirements:
- 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
Benefits:
- 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.
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