QA Manager, Data Integrity 80-100% (f/m/d)

Lonza; Oberwallis; On-site; Vertraulich; Full time

Job summary

Lonza in Visp, Switzerland, is seeking a Data Integrity professional to support governance, sustain ALCOA+ adherence, and drive site-wide compliance across GMP processes. You will collaborate with the Site Data Integrity Lead and cross-functional teams to implement DI standards and lead improvement initiatives.

The role emphasizes DI awareness, regulatory alignment, and proactive risk-based approaches, with opportunities to deputize the DI Community and coordinate stakeholder engagement at the

Qualifications

• Academic degree as listed in the job requirements.
• Experience in GMP-regulated pharma/biotech environments.
• Strong knowledge of Data Integrity principles and ALCOA+.

Responsibilities

• Support Data Integrity governance and site DI standards.
• Promote awareness through training and engagement with site functions.
• Plan, coordinate, and support Data Integrity walkthroughs at Visp.
• Support DI assessments, remediation, and continuous improvement across GMP processes.
• Provide DI support for deviations, investigations, change controls, CAPAs, QA activities.

Skills

Data Integrity

ALCOA+

GMP experience

Cross-functional collaboration

English fluency

Regulatory awareness

Education

Life Sciences degree

Engineering degree

IT/Computer Science degree

Pharmaceutical Sciences degree

Quality Management degree

Tools

Computerized systems

Quality systems

Job description

Switzerland, Visp

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

You will support the site's Data Integrity (DI) program at one of the largest biologics manufacturing sites in the world, where reliable, complete, and accurate data is essential to ensuring product quality, patient safety, regulatory compliance, and operational excellence.

In this role, you will work closely with the Site Data Integrity Lead and cross-functional stakeholders to support Data Integrity governance, promote ALCOA+ principles, support continuous improvement activities, and help maintain a sustainable state of compliance across the Visp site.

What You Will Get

• A place in an inclusive, dynamic, and passionate team, with the opportunity to contribute to the site's Data Integrity program and collaborate with cross-functional stakeholders across a diverse GMP manufacturing environment.
• An agile career and a dynamic work culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.

What You Will Do

• Support the site's Data Integrity governance program and contribute to the implementation of DI standards, initiatives, and site-specific improvement activities.
• Promote Data Integrity awareness and ALCOA+ principles through training programs, coaching, and engagement with site functions across Visp.
• Plan, coordinate, and support the execution of Data Integrity Walkthroughs across the Visp site and drive follow-up actions as required.
• Support and coordinate Data Integrity assessments, remediation activities, and continuous improvement initiatives across GMP processes on site.
• Provide Data Integrity support for deviations, investigations, change controls, CAPAs, quality risk assessments, audits, and inspections.
• Deputize the Visp Data Integrity Community and act as deputy for the Site Data Integrity Lead, facilitating community meetings, stakeholder engagement, and site-wide alignment activities as required.

What We Are Looking For

• Academic degree in Life Sciences, Engineering, Information Technology, Pharmaceutical Sciences, Quality Management, or another relevant discipline.
• Experience in a GMP-regulated pharmaceutical, biotechnology, or healthcare environment.
• Good understanding of Data Integrity principles, ALCOA+, computerized systems, and applicable regulatory requirements.
• Experience with quality processes, including deviations, investigations, CAPAs, change controls, and risk assessments.
• Ability to identify compliance risks, evaluate issues, and support the implementation of effective and pragmatic solutions.
• Strong communication and collaboration skills with the ability to work effectively in cross-functional teams.
• Experience supporting Data Integrity, compliance, computerized systems, CSV, Quality Systems, or related GMP activities.
• Experience supporting audits, inspections, or regulatory interactions is desirable.
• Fluency in English is required; German is an advantage.

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.

Reference: R79415