Team Lead CQV 80-100% (m/f/d)

If required, support for relocation is available to eligible candidates and their families. As Team Lead CQV - Specialized Modalities 80-100% (m/f/d) in Visp, you will take over the technical and organizational leadership of a CQV team and ensure the successful planning, coordination, and implementation of qualification activities for equipment, systems, and processes. In doing so, you will ensure compliance with regulatory requirements as well as the sustainable further development of the team and organization. This position requires full on-site presence. Personal collaboration enables close coordination in real time and ensures the technical precision required for the manufacture of medicinal products according to the highest quality and safety standards. What we offer you: An agile career and a dynamic work culture; An inclusive and ethical workplace; Compensation programs that recognize high performance; In addition to a competitive salary, numerous benefits in the areas of lifestyle, family, and leisure await you. You can also find the complete list of our global benefits at: Benefits - Visp. Your tasks: Technical and organizational leadership of a CQV team. Responsibility for the planning, coordination, and monitoring of qualification activities (DQ, IQ, OQ, PQ) for complex equipment, devices, and systems in close cooperation with Engineering, Production, QA, and other stakeholders. Management of external service providers and suppliers as well as taking on escalation responsibility for technical, organizational, and compliance-relevant topics. Promotion of the technical further development of the team through coaching, knowledge management, structured onboarding, and the building of a performance-oriented team culture. Support of audits and inspections as well as ensuring the long-term availability of critical CQV competencies in alignment with site and business strategies. Your qualifications: Completed studies (HF, FH, ETH) in engineering, biotechnology, pharmacy, or a comparable technical or scientific field. Sound experience in the technical and organizational leadership of teams as well as in the management of complex CQV projects and multidisciplinary stakeholders. Strong leadership, communication, and organizational skills as well as a high sense of responsibility and assertiveness. Several years of experience in the area of commissioning, qualification, and validation (CQV) of equipment, systems, and processes within a regulated environment. Sound knowledge in the creation and execution of qualification documentation (DQ, IQ, OQ, PQ), risk analyses, and regulatory requirements (GMP/GxP). Very good German and English skills in spoken and written form. About Lonza: At Lonza, our employees are our greatest strength. At over 30 sites on five continents, our globally networked teams work together every day to manufacture the medicines of tomorrow. Our core values: Collaboration, Accountability, Excellence, Passion, and Integrity reflect who we are and how we work together. The ideas of every individual, whether large or small, have the potential to improve millions of lives, and that is exactly what we want you to be a part of. Innovation thrives when people from diverse backgrounds bring their unique perspectives. At Lonza, we value diversity and are committed to an inclusive environment for all employees. If you are ready to turn our customers' groundbreaking ideas into actionable therapies, we look forward to welcoming you on board. Ready to shape the future of Life Sciences? Apply now