Deviation Manager in Visp

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.

Apply now

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Job profile

Life Sciences - Quality Management
Wallis
Contracting
Full Time
Immediately - 31.08.2026
Quality Assurance, deviation, CAPA

Sounds interesting? Simply click "Apply now" and I will get back to you.

Agnieszka Kawalec
Talent Acquisition Consultant
+41 41 632 43 54
Agnieszka.Kawalec@coopers.ch
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.

Firma: Coopers Group AG

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