Compliance Partner

at  Ferrosan Medical Devices

COMPLIANCE PARTNER – TI EXTERNAL ENGINEERING

Do you want to be a part of an engineering project team in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here, you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!

QUALIFICATIONS

It is expected that you hold an academic degree in Engineering, Pharmacy or similar. You must be able to work in a structured and analytical way. You have a strong quality mindset and can finish tasks before the deadline. To be successful in the job, it is important that you can collaborate with colleagues and that you are confident in challenging stakeholders at different levels.

TO BE SUCCESSFUL IN THIS ROLE, YOU WILL PROBABLY:

• Have experience within a pharmaceutical or medical device company with outsourced processes.
• Experience with analyzing data and applying it to problem solving and procedure development.
• Experience with project management is an advantage.
• Be familiar with writing documents and procedures in adherence to current regulations.
• Experience with audit preparation and execution.
• Have exceptional collaboration- & stakeholder management skills.
• Speak and write English fluently.

WE OFFER A TRULY PURPOSE DRIVEN WORKPLACE WHERE YOU CAN HAVE REAL IMPACT

We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun

More specifically, your main tasks will be:

• Optimize supplier- and CMO compliance set-up through cost-efficiency and quality parameters.
• Lead and participate in compliance improvement projects.
• Identify compliance gaps and participate in compliance activities that aim to close compliance gaps.
• Participate in and follow up on actions from the compliance network in FeMD.
• Document and manage changes and deviations in our QMS.
• Develop and optimize procedures and instructions