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Qualification & Validation Engineer

Borer Chemie AG

Employment type
Full-time
Location
Zuchwil
Company
Borer Chemie AG, Gewerbestrasse 13, 4528 Zuchwil
First posted
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Qualification & Validation Engineer (all genders) Chemistry, Process, Effect – everything from one source Borer Chemie AG is a globally active family-owned company based in the Espace Mittelland. For over 60 years, we have been synonymous with the highest level of competence in the demanding cleaning and disinfection of surfaces, instruments, and components. Our products are used wherever precise cleanliness is crucial: in hospitals, the life-sciences industry, medical technology, and in demanding industrial applications. As an employer, we offer short decision-making paths and a great deal of creative leeway. Those who work for us contribute to something that matters with their expertise. In a cross-functional role, we are looking for a reliable, meticulous, and self-employed as well as motivated personality as Qualification & Validation Engineer (all genders) •100% available immediately or by agreement • permanent position • Borer Chemie AG, Zuchwil Your area of responsibility In this function, you will report directly to the Director RQS and take on the following main tasks: Independent planning, coordination, and execution of qualification and validation activities in the GMP-regulated, chemical, or pharmaceutical industry as well as in the MedTech industry Ensuring a structured project flow as well as coordination with interdisciplinary departments such as RQS, QA, F&E, SCM/Operations, and external partners Carrying out qualifications on chemical plants, production infrastructure, and production-related equipment based on existing production processes Providing technical advice to internal stakeholders regarding compliance, qualification strategies, and regulatory requirements Moderating technical meetings as well as solution-oriented processing of project-related questions and deviations with involvement of the change control processes Reviewing, updating, and approving relevant documentation and specifications as well as assisting in their creation Your profile Completed degree or technical training in the fields of pharmaceutical, process, mechanical, electrical, or biotechnology or comparable qualification Several years of experience in qualification and validation within the pharmaceutical, chemical, or MedTech industry Good knowledge of relevant regulations and guidelines such as GMP, GxP, FDA, EU-GMP-Guideline, GAMP5 as well as Annex 1, 11, and 15 and MDR Experience in handling risk analyses, SOP creation, deviation management, and CAPA processes Secure handling of QMS, ERP, and documentation systems Structured, independent, and quality-oriented way of working with high accuracy and reliability Communication strength as well as experience in collaboration with interdisciplinary teams and customers Very good German language skills and good English language skills in writing and speaking Your benefits A diverse range of tasks with exciting challenges Flexible working hours Various team events Participation in training and further education Participation in fitness subscription Discount on Reka checks Hot and cold drinks as well as break fruits Charging station for e-vehicles Questions about the position For technical questions, Dr. Hendrik Demuth, Director RQS, is available by email. Your next step Does this sound like your next challenge? Then we look forward to your application. Apply now Loepfe Team Leader HR Borer Chemie AG - Gewerbestrasse 13 - 4528 Zuchwil / Switzerland

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Posted 1 week ago

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