Head of CQV/CSV - Advanced Synthesis Conjugates in Visp (80-100%) (m/f/d)

Lonza; Zermatt; Vor Ort; Vertraulich; Vollzeit

Zusammenfassung

A global pharmaceutical company in Switzerland seeks a Leader for CQV/CSV strategies. The role involves mentoring teams, ensuring compliance with cGMP regulations, and driving quality during equipment validation processes. Ideal candidates will have strong backgrounds in engineering, excellent communication skills, and fluency in German and English. Join a company that values diverse perspectives and collaborates to innovate and improve lives. Apply now to shape the future of life sciences.

Leistungen

Relocation assistance

Dynamic working culture

Inclusive workplace

Lifestyle and leisure benefits

Competitive salary

Aufgaben

• Lead, mentor, and develop a team of CQV, CSV specialists.
• Define and implement the CQV/CSV strategy for facilities.
• Provide expertise for equipment and utilities.
• Make strategic decisions on CQV/CSV standards.
• Ensure quality in commissioning and validation.
• Support audits and inspections as SME.
• Drive continuous improvement across functions.

Kenntnisse

Leadership in CQV/CSV

cGMP knowledge

Engineering and manufacturing processes

Team orientation

Strong communication skills

Organizational skills

Motivation and drive

Fluency in German and English

Jobbeschreibung

Relocation assistance is available for eligible candidates and their families, if needed.

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 on bit.ly/3wjkoFi

What you’ll do:

• Lead, mentor, and develop a team of CQV, CSV, and small‑device specialists, including hiring and qualification.

• Define and implement the CQV/CSV strategy for Advanced Synthesis Conjugates facilities in alignment with the Lonza Visp site.

• Provide CQV/CSV expertise for equipment, utilities, clean rooms, and small devices, acting as the interface between engineering and operations.

• Make strategic decisions on CQV/CSV standards and approaches during project engineering phases.

• Ensure quality and compliance in commissioning, qualification, validation, and support GMP risk assessments.

• Serve as SME for designated areas, support audits and inspections, and contribute to CQV standards development.

• Manage resources, drive continuous improvement, and maintain strong communication and collaboration across Manufacturing, QA, QC, Support Functions, and Engineering.

What we are looking for:

• Proven leader in CQV/CSV within biopharma or advanced synthesis environments.

• Strong background in cGMPs.

• Proficient knowledge of engineering and manufacturing processes.

• Proven leadership skills with a strong team orientation.

• Outstanding communication skills for internal and external interactions.

• Structured, focused, and well-organized working attitude.

• Agile, highly motivated, and driven to succeed.

• Proficient in German with strong English communication skills.

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.