Join MindCapture as a consultant where your process validation expertise can drive quality, compliance plus operational excellence in healthcare.
What is offered?
Ready to grow your career and make real impact? Join MindCapture!
We offer competitive salaries, a full benefits package with meal vouchers, eco vouchers, DKV health insurance, group insurance, net expense allowance plus a company car. You also get the opportunity to shape your future through personalised training plus development.
At MindCapture, you choose what you love, build on your strengths, and make a difference where it matters most.
You will work as a MindCapture consultant or freelancer for an international market leader in the healthcare industry.
Job Description:
* Support process validation activities for manufacturing processes in a regulated medical device environment
* Prepare validation protocols, support execution on the production floor and ensure clear reporting of results
* Help maintain the validated state of production processes and keep documentation complete and inspection ready
* Provide hands on QA support to production activities in line with ISO 13485 and internal quality standards
* Maintain and update work instructions, forms, batch records and related production documentation
* Support batch record review and incoming inspection of materials and components
* Follow up equipment maintenance, calibration and labelling from a quality and documentation perspective
* Contribute to the validation of process changes linked to equipment, materials and software
* Support the installation and validation of sensors used for production monitoring
* Assist in deviations, non conformities, CAPA and change control activities
* Work closely with QA, production and engineering teams to ensure compliant and practical processes
Requirements:
* Bachelor’s or Master’s degree in engineering, life sciences, biomedical sciences or a related technical field
* 3 to 5 years of experience in process validation, manufacturing quality or production QA in a regulated environment
* Strong knowledge of ISO 13485
* Experience with validation documentation, protocol writing, execution and reporting
* Familiarity with batch review, incoming inspection, deviations and change documentation
* Hands on, structured and quality minded with strong documentation skills
* Able to work closely with operational teams and translate quality requirements into practice
* On site presence of 4 days per week
Are you ready to make a real difference in healthcare?
Join our dynamic team and help drive innovation in medical devices.
Apply now and let’s make an impact together!
Want to learn more? Discover all .
If MindCapture sees a potential fit, we’ll get in touch as soon as possible.
If you don’t hear from us within two weeks, it simply means that this particular position wasn’t the right match. In that case, we’ll gladly keep your profile in mind for future roles that could suit you better.