Senior Quality Specialist
Technolution
Senior Quality Manager or Engineer who enjoy creating results through others?
Are you an experienced Quality Manager with a strong background in MedTech or Pharma, and do you feel energized in the role as project lead? Do you enjoy being the spider in the web, making things happen, and ensuring progress and success in the Quality Management-area? Then we have a spot-on position for you.
Don’t be careful what you wish for
Because we are quite confident to be able to grant all your wishes. Such as being part of an energetic team of very experienced Quality Managers. We are drivers and problem solvers, who eliminate road bumps that might occur in the projects, and we ensure our clients are compliant with the needed standards and regulations. You might not know all the standards and regulations by heart, but you know where to look, because you have seen it all before and know how to apply Quality Management in practice.
As a consultant, you will work on diverse projects with start-ups to industry leaders, some days from the office in Hørsholm, some days onsite at the clients and some days remote. And by the way: being a consultant at Technolution is not equivalent to being a lone wolf. You will always be part of a team, at the client’s or at Technolution. You will often collaborate with your colleagues from Usability Engineering, Design Control, Risk Management and Mechanical Engineering. We have a strong focus on continuously developing our skillset and staying up to date and since you will help us develop this area of expertise, we can’t wait to get to know you, and your toolbox.
We have a few wishes too
You have at least 5 years of experience working with Quality Management in Pharma or MedTech, you know that things are not black and white, and you have an intuitive understanding of how standards play out and how to apply them in a pragmatic and effective way. You thrive working with people, practice stakeholder management and you take a holistic view on things. In other words: you have a solid business understanding, and you are very familiar with standards such as ISO 13485, FDA and EU regulations for MD, IVD and Combination Products.
If you're ready to bring your expertise to a collaborative and dynamic setting, click the "Apply" button below and become a part of a Quality Management team with high aspirations and standards.
Department: Quality Management & RegulatoryDeadline: 05 January 2025
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