Associate Director, GE Commissioning & Qualification (CQ) Visp (80 100%) (m/f/d) Apply locations CH Visp time type Full time posted on Posted 3 Days Ago job requisition id R64057 Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, theres no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And thats the kind of work we want to be part of. We are hiring for a driven Global Engineering CQ Lead Shared Function (Commissioning, Qualification). In this role you will ensure that services and processes meet the regulatory requirements and quality standards. Join our ambitious team and help deliver world class engineering projects. This is an outstanding opportunity to contribute to innovative CQ project in Switzerland! The role is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role requires to be onsite full time. Key responsibilities: Responsible for handling and leading a team of CQ experts. Oversee the generation of all protocols for several projects such as life cycle documents. Commissioning and qualification plan and report. Oversee the alignment and execution of the IV/IQ static testing across all site projects. The GE CQ Lead shared function will mainly support all the CQ Portfolio lead but also collaborates with other departments, such as engineering, manufacturing, quality, procurement and regulatory affairs, to ensure that CQ activities are increasing efficiency regarding cost and timeline. Oversee several remote offices which will be located in different strategic locations across the globe to increase efficiency and reduce cost. Be in charge to assess the capability and capacity of all supplier quality departments to ensure delivery of proper documentation in a timely manner. Collaborate with the different CQ Portfolio lead to ensure alignment on the documentation across all VISP projects. Lead CQV activities to ensure compliance with regulatory requirements and industry standards. Collaborate with the different CQ Portfolio lead to ensure capacity of resources for document generation and static qualification activities such as IV/IQ. Collaborate with cross functional teams to identify and mitigate risks associated with CAPEX investments. Provide technical leadership and guidance for CQV activities according to industry standards. Develop and maintain relationships with key stakeholders for successful project execution. Key requirements: Master''s Degree or equivalent experience in Pharma, Engineering, or Science. Proven experience in Pharma / Engineering (GEP/GMP). Proven experience in Project Management, CQV. Proficient in English; German is an advantage. Understanding of Pharmaceutical/Bio Science