Deviation Investigator Manager (w/m/d)
Start date: 02/03/2026 - 30/06/2026
Location: Visp, Switzerland
Key Responsibilities
* Represents the Operations Unit, taking ownership of Deviations which arise; to investigate the root cause(s), the impact/potential impact on product and/or systems, and to define appropriate CAPA(s) as solutions.
* Responsible to own, author, record and investigate Deviations.
* Liaise with Subject Matter Experts (SMEs) and key stakeholders to establish the root cause(s) 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(s), 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.
Key Requirements
* Bachelor degree in chemistry, biotechnology, life science or related field.
* Previous experience in Deviations and cGMP in a regulated pharmaceutical/API industry is a strong advantage.
* 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.
* Demonstrated previous experience is a strong advantage.
* Structured, focused and well-organized working attitude.
* Open-minded for new ideas and suggestions; agile, highly motivated and dynamically driven.
SThree_Germany is acting as an Employment Business in relation to this vacancy.