Deviation Manager m/w/d, Wallis He/She represents the Operations Unit, taking ownership of Deviations which arise;
investigate the root cause, the impact/potential impact on product and/or systems, an
to define appropriate CAPA as solutions.
Location: Visp
Contract start date: 02/03/2026
Contract end date: 31/08/2026
Responsibilities: - Responsible to own, author, record and investigate Deviations.
- Liaise with Subject Matter Experts and key stakeholders to establish the root cause of deviations and the potential impact of said deviations.
- Ensure proper investigational tools are used to systematically define the root cause(s) and contributing factor(s) (e.g., Fault Tree Analysis, Defense Analysis, Event & Causal Factors Chart, Fishbone Diagram, etc.).
- Contribute to define appropriate CAPA, and associated Effectiveness Checks, as solutions to correct deviations and prevent future recurrence.
- Ensure cGMP compliance through the investigation process, and to drive their quality records to completion and timely closure.
- Support the business through ongoing change and process improvement activities.
Requirements: - Bachelor degree in chemistry, biotechnology, life science or related field.
- Previous experience in Deviations and cGMP in a regulated pharmaceutical/API industry.
- Knowledge of biotech. manufacturing processes and analytical methods is an advantage.
- Experience with Human and Organizational Performance & risk management approaches is an advantage
- Fluency in English, both written and spoken. German is an advantage.
- Technical writing & presentation/communication skills are key for the role.
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