The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
As an Associate Director CQV Integrated Biologics (80-100%) (m/f/d) in Visp, Switzerland, you will oversee the strategic planning, leadership, and execution of CQV activities to ensure biotech manufacturing systems meet regulatory and operational standards. This role requires strong leadership and deep expertise in GMP environments to guide cross-functional teams in delivering compliant, efficient facility start-ups and ongoing validation.
What you’ll get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits in Visp can be found onhttps://bit.ly/3wjkoFi
What you’ll do:
Lead a team of senior CQV experts, overseeing all aspects of human resource management including qualification, development, mentoring, hiring, pay decisions, and team issues, in alignment with the head of engineering biologics
Set up and manage a local group of CQV experts for biologics facilities, providing support to future operations users during periodic qualification.
Collaborate with your team on capital investment projects and improve operations teams with your expert CQV knowledge.
Engage in planning CQV activities to ensure accurate operations and resources are available for each project step, serving as the facilitator for all key collaborators.
Securing operations input to CQ (gate keeper), definition and standardization of PQ approach
Build and manage a pool of external resources and capabilities to support CQV operations.
Promote Lonza's culture of openness, cooperative teamwork, and continuous improvement even beyond your immediate responsibilities.
What we’re looking for:
Bachelor / Master / Diploma from a technical school (HF) / university of applied sciences (FH) or university in a technical field, or equivalent experience.
Extensive experience in the area of commissioning, qualification and validation (CQV) in a biotech related environment
Depth understanding of bioprocesses, GMP and biopharma production
Strong experience in CQV project management
Strong leadership skills (strong team orientation) and ability to communicate internally and externally at higher levels,
Strong business understanding in an CDMO environment
Fluent in English, German language skills are advantageous
About Lonza:
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.