Compliance Program Manager
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Søborg
Compliance Program Manager for global medical device producer
Ferrosan manufactures critical haemostatic products that are used in more than 100 countries globally, to help doctors minimise bleeding during surgeries. Ensuring that these products are compliant with quality requirements and regulation is vitally important for patients worldwide. We need you to take the lead on projects aiming to optimise our compliance efforts across Ferrosan.
A hand in the grand strategy
As compliance program manager, you join the leadership team along with the 3 managers from Quality Assurance, Quality Control and Regulatory Affairs, respectively, as well as 2 specialists. You will all be reporting to Camilla Hudtloff, VP of QM/RA.
The leadership team has the task of steering Ferrosan in the right strategic direction with regards to quality of product and compliance with regulation. You will be working across the leadership team, with the managers from each field, as well as other stakeholders internally in Ferrosan, guiding the various departments to ensure that compliance is maintained across all aspects of the company.
The beating heart of compliance
You will be the driving force behind a host of different initiatives, spearheading projects aiming at optimising the activities within each area with regards to compliance. The quality of our products is quite literally a matter of vital importance to lots of people worldwide, and compliance is a big part of maintaining that quality. In your role as compliance program manager, you can expect to be:
Real impact and room to grow
A seat at the leadership table and referring to a VP means you have very real impact on the scope and direction of the strategic foundation within Ferrosan. Not only are you a part of shaping the entire strategic aim, you will also be taking an active role in seeing the projects through.
Your tasks and projects vary a lot, as you are working within very different fields, and so your days will never be quite alike. This is an ideal environment in which to develop your competencies, and we highly prioritise your growth. When you get better, so do we.
An ambitious and autonomous diplomat
The most important factor in your success is that you are driven and can work independently. You will be working on various projects across multiple departments, so you must be an excellent collaborator. You are often working on cross-departmental projects, where you will have to get people with differing mindsets and motives to cooperate, so it is important that you are a natural communicator and stakeholder manager.
As to the specifics:
Interested?
Then send your application and CV no later than 19. Nov 2021. Make sure to mark your application with ‘Compliance Program Manager’.
If you wish to know more about your new job, feel free to contact VP QM/RA Camilla Hudtloff at +45 5213 2887.
Ferrosan manufactures critical haemostatic products that are used in more than 100 countries globally, to help doctors minimise bleeding during surgeries. Ensuring that these products are compliant with quality requirements and regulation is vitally important for patients worldwide. We need you to take the lead on projects aiming to optimise our compliance efforts across Ferrosan.
A hand in the grand strategy
As compliance program manager, you join the leadership team along with the 3 managers from Quality Assurance, Quality Control and Regulatory Affairs, respectively, as well as 2 specialists. You will all be reporting to Camilla Hudtloff, VP of QM/RA.
The leadership team has the task of steering Ferrosan in the right strategic direction with regards to quality of product and compliance with regulation. You will be working across the leadership team, with the managers from each field, as well as other stakeholders internally in Ferrosan, guiding the various departments to ensure that compliance is maintained across all aspects of the company.
The beating heart of compliance
You will be the driving force behind a host of different initiatives, spearheading projects aiming at optimising the activities within each area with regards to compliance. The quality of our products is quite literally a matter of vital importance to lots of people worldwide, and compliance is a big part of maintaining that quality. In your role as compliance program manager, you can expect to be:
- Driving optimisation of existing processes, such as deviations, changes, and CAPAs
- Contributing to the development of data management to support daily compliance
- Driving development of new training set-ups within Quality Assurance, Quality Control, and Regulatory Affairs
- Supporting the Quality Assurance, Quality Control, and Regulatory Affairs departments with projects and activities
Real impact and room to grow
A seat at the leadership table and referring to a VP means you have very real impact on the scope and direction of the strategic foundation within Ferrosan. Not only are you a part of shaping the entire strategic aim, you will also be taking an active role in seeing the projects through.
Your tasks and projects vary a lot, as you are working within very different fields, and so your days will never be quite alike. This is an ideal environment in which to develop your competencies, and we highly prioritise your growth. When you get better, so do we.
An ambitious and autonomous diplomat
The most important factor in your success is that you are driven and can work independently. You will be working on various projects across multiple departments, so you must be an excellent collaborator. You are often working on cross-departmental projects, where you will have to get people with differing mindsets and motives to cooperate, so it is important that you are a natural communicator and stakeholder manager.
As to the specifics:
- We expect that you have many years of experience within quality assurance, preferably with QC and RA experience as well, and ideally within the field of medical devices
- We expect that you have tangible experience with managing projects
- We would prefer that you have a background in the pharmaceutical or medical device industries
- We would prefer that you have knowledge with ISO 13485 and Medical Device Regulation (EU) 2017/745, and that you know the requirements for being in compliance
- We would prefer that you have experience with Lean thinking
Interested?
Then send your application and CV no later than 19. Nov 2021. Make sure to mark your application with ‘Compliance Program Manager’.
If you wish to know more about your new job, feel free to contact VP QM/RA Camilla Hudtloff at +45 5213 2887.
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 4.11.2021, 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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