Qualification & Validation Engineer
- Employment type
- Full-time
- Location
- Zuchwil
- Company
- Borer Chemie AG, Gewerbestrasse 13, 4528 Zuchwil
- First posted
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