Lonza

Quality Site Head

Lonza  •  €90k - €126k/yr  •  Köln, DE (Onsite)  •  1 hour ago
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Job Description

Job Title: Quality Site Head

Location: Cologne

Relocation support is available for the successful candidate.

The role:

This role is accountable for leading quality and compliance oversight across all product lifecycle activities at Lonza Cologne, ensuring full adherence to EU-GMP standards. It oversees both Quality Control and Quality Assurance functions, including product testing, quality systems, and the compliant release of products, while leading and developing a team of up to 12 staff to drive performance and a strong quality culture.

The position serves as the site’s Quality representative, partnering closely with cross-functional and corporate teams and holding final decision-making authority on product approval or rejection. It also provides leadership and support to Operations and QC teams to address performance and compliance challenges, while maintaining robust quality documentation, guiding site procedures, and ensuring readiness for internal and external audits.

This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get:

  • An agile career and dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • A variety of benefits dependant on role and location

  • The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits

The full‑time annual base pay for this position in Cologne is expected to range between €90,000 and €126,000. Initial salary placement within this range will be determined based on role‑related factors such as experience, qualifications, and expected contribution.

What you will do:

  • Lead quality and compliance oversight across all site activities, ensuring adherence to EU-GMP and ISO)

  • Oversee Quality Control and Quality Assurance functions, including coordination of product testing and final approval or rejection decisions

  • Provide strategic quality leadership and expert support to Operations and QC teams to resolve performance and compliance issues

  • Act as the site Quality Representative, collaborating with cross-functional teams and corporate quality

  • Maintain and improve the site’s Quality Management System, including SOPs, processes, and quality documentation

  • Ensure audit readiness and support the preparation and execution of internal, external, and regulatory audits.

  • Drive quality performance management, including KPIs, management reviews, and continuous improvement initiatives

  • Manage quality-related processes such as deviations, CAPAs, change controls, and investigations to ensure timely resolution and compliance.

What we are looking for:

  • Extensive experience (10+ years) in Quality, GMP-regulated environments, ideally within biotech, pharmaceuticals, or life sciences.

  • Extensive leadership experience in Quality Assurance, Quality Control, and Regulatory Compliance.

  • Deep expertise in EU-GMP, ISO 13485 and regulatory frameworks, with strong knowledge of quality systems and compliance requirements.

  • Proven leadership capability, including managing teams, driving performance, and influencing cross-functional stakeholders.

  • Strong decision-making and accountability, particularly in product release, deviations, CAPAs, and quality risk management.

  • Strategic mindset with operational excellence, able to lead audits, drive continuous improvement, and maintain inspection readiness at all times

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.

Lonza

About Lonza

Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.

Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.

For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Basel, CH
Year Founded
1897
Website
lonza.com
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