Engineer Qualification and Validation

Engineer Qualification & Validation - GMP / Validation / Pharma / Plants Background: You don't just want to manage documentation, but contribute directly to the stability, compliance, and further development of our production with your expertise? Then this role is for you. In our team, we are responsible for the qualification and validation of our manufacturing equipment. This makes us an important partner for routine production and for improvements to existing plants and processes. For our location in Rotkreuz, we are looking for a personality who likes to take responsibility, works close to production, and pragmatically advances technical and compliance-related topics. The perfect candidate: The perfect candidate has a completed degree in natural or engineering sciences and two to three years of solid professional experience in qualification and validation in the regulated pharma or medical technology field. Additionally, they are characterized by a structured, independent way of working, strong communication skills in German and English, and the competence to accompany complex production projects and audits in a sovereign manner. Tasks & Responsibilities: • You plan and coordinate qualifications of small equipment up to complex production plants. • You create and moderate risk analyses and derive suitable measures from them. • You support process and method validations as well as requalifications and revalidations in the event of changes. • You actively work on improvement projects in our existing production. • You analyze disturbances, deviations, and technical issues in the production environment together with specialist departments. • You assess together with internal partners when qualification or validation needs exist. • You coordinate independently with various stakeholders and keep topics reliably moving. • You support audits technically and represent your area of responsibility in a sovereign manner. • You ensure that regulatory requirements and internal quality standards are met. Must Haves: • A completed degree in natural sciences, engineering sciences, or a comparable field • 2-3 years of experience in a regulated environment, for example in pharma, diagnostics, medical technology, or a similar industry • Practical experience in the qualification of equipment or plants • Knowledge of process and method validation is a plus • Experience with quality-relevant documentation and risk analyses • Technical understanding and interest in production-related topics • A structured, independent, and proactive way of working • Enjoyment of collaboration in interdisciplinary teams • Very good German language skills and good English language skills Reference Nr.: 925071SBI Role: Engineer Qualification & Validation Industry: Pharma Location: Rotkreuz Percentage: 100% Working hours: Standard (hybrid model) Start: ASAP-01.12.2026 Duration: unlimited Application deadline: 13.07.2026 If this position has sparked your interest, please send us your complete dossier via the link in this advertisement. If this position does not fit your profile so well and you wish to receive other positions directly, you can also send us your dossier via this advertisement or to jobs[at]itcag[dot]com. Contact us for further information about our company, our positions, or our attractive Payroll-Only-Program: +41 41 760 77 01. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with branches in Germany and Ireland. ITech Consult specializes in the placement of IT candidates for contract work. We were founded in 1997 by IT professionals and therefore know how important professional support is when searching for and working on projects.