CQV Engineer / Qualification & Validation Engineer 80-100% (m/f/d)

Lonza

Oberwallis

Remote

CHF 110,000 - 150,000

Full time

2 days ago
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Benefits offered by this job

Dynamic career & work culture
Inclusive and ethical workplace
Competitive compensation programs
Lifestyle, family and leisure benefits

Job summary

Lonza in Visp, Switzerland, is seeking a CQV Engineer / Qualification & Validation Engineer (m/f/d) to qualify and validate new process equipment and facilities, supporting continuous improvement and excellence in operations.

You will develop commissioning and qualification documents, oversee deviations and CAPAs in a GMP environment, and coordinate with internal teams and external providers to ensure compliant project execution.

Qualifications

  • Graduate from HF/FH or university (or equivalent) with GMP exposure.
  • Proven experience in GMP environments, commissioning, qualification and validation of systems.
  • Familiarity with MS Office; COMOS, DMS, Kneat, TrackWise and SAP is advantageous.
  • Proficient in written and spoken German and/or English.
  • Demonstrate independent, flexible work habits with strong communication and a structured, proactive approach.

Responsibilities

  • Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems.
  • Supervise and resolve deviations, manage changes (GEP and GMP), and implement CAPAs effectively.
  • Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution.
  • Present qualification documents during audits and inspections, showcasing the outstanding standards maintained.

Skills

German language
English language

Education

HF/FH or university degree

Tools

MS Office
COMOS
DMS
Kneat
TrackWise
SAP

Job description

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

Join our team at Lonza in Visp, Switzerland as a CQV Engineer / Qualification & Validation Engineer (m/f/d). Work alongside an outstanding team dedicated to maintaining flawless operations and premier standards. This role provides an exciting chance to contribute to our dynamic environment, directly improving the quality and efficiency of our processes. Take part in qualifying and validating brand-new process engineering equipment and facilities, promoting continuous improvement and innovation.

  • An agile career and a dynamic work 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. The full list of our local tailored benefits in Visp: Benefits - Visp
What you will do:
  • Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems and ongoing SLC support post-implementation.
  • Supervise and resolve deviations, manage changes (GEP and GMP), and implement CAPAs effectively.
  • Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution.
  • Present qualification documents during audits and inspections, showcasing the outstanding standards maintained.
What we are looking for:
  • Graduate from a technical school (HF) / university of applied sciences (FH) or hold a university degree
  • Proven experience in a regulated GMP environment, specifically in commissioning, qualification, and validation of systems like refrigerators, freezers, clean media, and process engineering equipment
  • Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP is advantageous
  • Proficient in both written and spoken German and/or English
  • Demonstrate independent, flexible work habits, with excellent communication skills and a structured, focused approach to tasks.
  • Open to new ideas, agile in thinking, and proactive in problem-solving.
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.

  • Take ownership, step forward, and enjoy meaningful responsibility
  • Love solving problems and thrive in a complex, fast-moving environment
  • Are curious, always looking to learn and improve
  • Work collaboratively, contributing to something bigger than yourself
  • Are motivated to make a difference through work that impacts customers and their patients
Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.

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