Deviation Specialist at Visperterminen, Visp

Details of the job offer

  2026-07-27
  Full time
  Temporary
Gi Group co-branding

For a biopharmaceutical company based in Visp and specialized in the production of biological drugs in mammalian cell culture, our team is looking for a Deviations Specialist to strengthen its quality activities in GMP environment.

-      Contract : Temporary

-      Start date : Beginning of August

-      Duration : 5 months


Deviation Specialist 2 - Temporary position

Primary mission

The Deviations Specialist is responsible for the management, investigation and closure of deviations occurring in a GMP biopharmaceutical environment, particularly within a large-scale mammalian cell culture facility. He/she acts as the representative of Operations and ensures the identification of root causes, the evaluation of quality impacts, and the implementation of effective CAPA.


• Write, record, track, and close quality deviations.

• Ensure document compliance throughout the deviation’s life cycle.

• Ensure compliance with processing and closing times.

• Conduct investigations to identify root causes and contributing factors.

• Collaborate with business experts (SME) and relevant stakeholders.

• Assess the actual or potential impact on products, processes, equipment, or quality systems.

• Use structured problem-solving methodologies (root cause analysis, quality risk management tools)

• Define and implement corrective and preventive actions.

• Establish efficiency criteria and controls.

• Monitor the execution of CAPAs to prevent recurring events.

• Participate in change and process optimization projects.

• Contribute to strengthening the quality culture and GMP compliance.

• Support operational improvement initiatives.


Profile :

• Bachelor’s degree in Chemistry, Biotechnology, Life Sciences or equivalent scientific field.

• First experience in deviation management and GMP/cGMP environment within the pharmaceutical, biotechnology, or API industry, highly appreciated.

• Knowledge of biotechnological manufacturing processes and associated analytical methods.

• Experience in root cause analysis, risk management, and Human & Organizational Performance (HOP) approaches is an asset.

• Excellent command of English (spoken and written); German is a plus.

• Strong writing, analytical and communication skills.

• Organized person, rigorous, proactive and solution-oriented, able to work effectively with multidisciplinary teams in a dynamic and regulated environment.

• English: fluent (written and oral), German is a must.

  Biopharmaceutical
  Pharmaceutical and biotechnology
  14998

Deviation Specialist
Temporary / Visperterminen
Place of work - City:
Visperterminen
Industrial sector:
Biopharmaceutical
Professional area:
Pharmaceutical and biotechnology
Number of vacancies:
1
Reference code:
20662
Salary per:
Job offer insertion date:
2026-07-27

For a biopharmaceutical company based in Visp and specialized in the production of biological drugs in mammalian cell culture, our team is looking for a Deviations Specialist to strengthen its quality activities in GMP environment.

-      Contract : Temporary

-      Start date : Beginning of August

-      Duration : 5 months


Deviation Specialist 2 - Temporary position

Primary mission

The Deviations Specialist is responsible for the management, investigation and closure of deviations occurring in a GMP biopharmaceutical environment, particularly within a large-scale mammalian cell culture facility. He/she acts as the representative of Operations and ensures the identification of root causes, the evaluation of quality impacts, and the implementation of effective CAPA.


• Write, record, track, and close quality deviations.

• Ensure document compliance throughout the deviation’s life cycle.

• Ensure compliance with processing and closing times.

• Conduct investigations to identify root causes and contributing factors.

• Collaborate with business experts (SME) and relevant stakeholders.

• Assess the actual or potential impact on products, processes, equipment, or quality systems.

• Use structured problem-solving methodologies (root cause analysis, quality risk management tools)

• Define and implement corrective and preventive actions.

• Establish efficiency criteria and controls.

• Monitor the execution of CAPAs to prevent recurring events.

• Participate in change and process optimization projects.

• Contribute to strengthening the quality culture and GMP compliance.

• Support operational improvement initiatives.


Profile :

• Bachelor’s degree in Chemistry, Biotechnology, Life Sciences or equivalent scientific field.

• First experience in deviation management and GMP/cGMP environment within the pharmaceutical, biotechnology, or API industry, highly appreciated.

• Knowledge of biotechnological manufacturing processes and associated analytical methods.

• Experience in root cause analysis, risk management, and Human & Organizational Performance (HOP) approaches is an asset.

• Excellent command of English (spoken and written); German is a plus.

• Strong writing, analytical and communication skills.

• Organized person, rigorous, proactive and solution-oriented, able to work effectively with multidisciplinary teams in a dynamic and regulated environment.

• English: fluent (written and oral), German is a must.


https://ch.gigroup.com/job-offer-detail/visperterminen-visp-deviation-specialist/20662/