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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