Compliance Partner
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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!
Securing compliance of our suppliers and CMOs
Our new compliance partner will play a pivotal role in raising the bar for the overall quality level and ensuring a high level of compliance of our suppliers and CMOs. To be successful in the job, it is important that you can collaborate with colleagues in different functions and have strong communication skills. You will also be assigned tasks that require you to work on your own and without detailed instruction – which is why your ability to take initiative is a key trait in your professional toolbox. Being responsible for many aspects regarding compliance, you can present complex results to stakeholders with different levels of understanding.
More specifically, your main tasks will be:
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:
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 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV at the latest on August 31, 2024. We will process the applications as we receive them.
Questions? Please do not hesitate to contact us:
Camilla Kromann Sisden
Manager, TI External Engineering
+45 29 92 19 87
We look forward to hearing from you.
Read more about us here
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!
Securing compliance of our suppliers and CMOs
Our new compliance partner will play a pivotal role in raising the bar for the overall quality level and ensuring a high level of compliance of our suppliers and CMOs. To be successful in the job, it is important that you can collaborate with colleagues in different functions and have strong communication skills. You will also be assigned tasks that require you to work on your own and without detailed instruction – which is why your ability to take initiative is a key trait in your professional toolbox. Being responsible for many aspects regarding compliance, you can present complex results to stakeholders with different levels of understanding.
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.
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 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV at the latest on August 31, 2024. We will process the applications as we receive them.
Questions? Please do not hesitate to contact us:
Camilla Kromann Sisden
Manager, TI External Engineering
+45 29 92 19 87
We look forward to hearing from you.
Read more about us here
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 1.7.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Søborg
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