Join MindCapture as a consultant where your process validation expertise can drive quality, compliance plus operational excellence in healthcare.
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.
You will work as a MindCapture consultant or freelancer for an international market leader in the healthcare industry.
Support the development, execution plus follow up of process validation activities for manufacturing processes in a regulated medical device environment
Provide hands on QA support to production teams to ensure activities are performed in compliance with internal procedures plus applicable quality standards
Work closely with operators plus manufacturing stakeholders to strengthen quality awareness plus ensure procedures are practical plus effective
Ensure process related documentation is aligned with ISO 13485 requirements plus internal quality system expectations
Contribute to change control, CAPA plus continuous improvement activities related to process performance plus product quality
Help ensure validation plus QA activities are performed in a structured plus compliant manner, with strong attention to traceability plus documentation quality
Collaborate with QA, production, engineering plus other internal stakeholders to align validation activities with operational needs
Act as a practical plus structured quality partner on process level, bridging shop floor realities with quality plus compliance requirements
Support improvement initiatives by translating process observations into concrete quality plus validation actions
Bachelor’s or Master’s degree in engineering, life sciences, biomedical sciences or a related technical field
Minimum 3 to 5 years of experience in process validation, manufacturing quality or production QA within the medical device industry or another highly regulated environment
Experience supporting QA activities in a production environment including work instructions, deviations plus change documentation
Structured, hands on plus quality minded professional with strong documentation skills
Good communication skills plus the ability to work effectively across QA, production plus technical teams
Join our dynamic team and help drive innovation in medical devices.