Quality manager (m/f/d)

Role Summary

Our goal is to close chronic wounds sustainably instead of simply treating wounds.

As a multi-award-winning, young MedTech company, we have managed to take wound care to the next level with our new, innovative treatment approach and be able to help many patients in the process.

That is exactly our drive and motivation. We look forward every day to appreciative interaction with each other, flat hierarchies for the implementation of projects, space for creative ideas and our further development, exciting tasks, our sense of humor and the feedback from numerous patients who tell us about their closed wounds.

As part of our QM department, you will play a crucial role on our path to becoming the leading provider of add-on wound therapies.

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Your motivation and a meaningful CV &

Your salary expectations

We look forward to getting to know you!

💬 Any questions?

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• #Quality Management #Quality Control #Quality Assurance
• #QM representative #QualityManager
• #Quality Engineer #Quality Management Representative #Quality Inspector
• #Quality Management Specialist #QMB
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Responsibilities

You support our QMB in day-to-day business and work together as a team to further develop our quality management system in all areas - including for Europe and the USA

• You carry out internal audits and support external audits and inspections by notified bodies and authorities at national and international levels
• Coordination and tracking of CAPA processes
• Together with your colleagues, you will ensure that our innovative products are and remain safe to use around the world
• In addition to the QMB, you also support the areas of production, R&D and regulatory affairs in QM-relevant issues

Requirements

• You have successfully completed your university studies with a focus on medical technology, regulatory affairs or a comparable qualification
• You have at least 3 years of professional experience in the area of quality management at a medical technology manufacturer
• You have relevant knowledge of standards and regulations (such as FDA, MDR and ISO 13485)
• Experience with different sterilization processes complements your profile, but is not a must
• You are confident in using MS Office
• You are a team player with a structured, detail-oriented, independent and results-oriented way of working
• Fluent German and English skills, both spoken and written, round off your profile

Benefits

• Flat hierarchies, open communication and genuine cooperation characterize our corporate culture
• A working environment in which you can keep the focus, help shape it and develop your full potential
• Continuous training and qualification opportunities individually tailored to you
• Flexible working time models and the opportunity to work mobile
• 30 days vacation per year
• A permanent job with performance-based pay and extras tailored specifically to you

🎤 Now it's your turn!