* Life Sciences - Quality Management * Wallis * Contracting * Vollzeit * Immediately - 31.08.2026 * Quality Assurance, deviation, CAPA 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.