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Would you like to work with products that change the lives of hearing-impaired people and do it in a worldwide, fast-growing company? And do you have experience with compliance in a quality and regulatory affairs environment? Then you could be the person we are looking for as our new Compliance Specialist.
You will join a leading supplier of premium diagnostic audiological equipment used every day in hearing clinics and hospitals around the world. From our headquarters we sell to more than 100 countries through our own sales companies and external distributors, and we are part of the global hearing healthcare company Demant.
Ensure documentation of medical device products
We are on an exciting growth path and right now we are enhancing our capabilities in our Regulatory Compliance Team. If you are looking for a job in a top professional informal organization, this is the perfect place to do so!
Through your position you will have an immediate impact on regulatory compliance and future product development and launch. You will ensure our product compliance administration and maintenance of standard product documentation delivering valuable information to the regulatory department which ensures the right external product registration.
Ensuring new standards and recertification
As a team member in the compliance team, you will also be involved in regulatory surveillance and safety related risk analysis ensuring new standards and recertification are handled and new standards implemented in our knowledge base.
Working side-by-side with our developers and regulatory compliance team members, you will be responsible for and delivering:
Process security tests Prepare reports to support regulatory requirements for medical devices, such as risk analyzes, usability reports, material evaluations and the like Actively engage with our regulatory team and support with applications around the world Monitor international standards for medical devices in the area of safety Actively support our design teams with evaluations and support
Furthermore, the job is also to continuously improve our compliance process and following up on the latest new requirements.
Your contribution
Using your solid knowledge about product documentation, and requirements in the different markets you cooperate with project teams ensuring a smooth compliance process in line with the overall project plans.
We are looking for a candidate with a proven track record of regulatory compliance from a similar position which has involved documentation of electrotechnical, wireless products.
Being able to succeed, you should be familiar with regulations and processes for electrotechnical products such as risk analysis and familiar with international standards for medical devices
As a person it is crucial that you are diplomatic and able to coordinate the activities of the people around you. Ensuring structure and being systematic of course comes natural to you. Finally, you care about the details, and you have a "can-do" attitude.
Join our fantastic compliance department in Global Quality
You will be placed at our Interacoustics headquarters in Middelfart which is just one of many global brands that you will be working with. The other brands are placed in the UK, USA, and Germany.
At Interacoustics you meet all R&D disciplines under one roof. The compliance team is part of the quality organization and works closely with the development teams in R&D. Global Quality consist of 16 colleagues in total. Joining the compliance department, you will be part of a team of 4 people and on a daily basis, you will be reporting to our Compliance Manager.
We are based in a modern and open building where flexible work environment, knowledge-sharing and mutual professional respect making it fun and meaningful to be here. We all share the passion and the strong will to deliver premium quality in everything we do.
Do you want to join the team or learn more about the position?
Then send your CV and cover letter as soon as possible.
For more information about the position please contact Allan KARSBERG from KARSBERG Recruitment & Headhunting at +45 2113 2169.
We look forward to hearing from you.
You will join a leading supplier of premium diagnostic audiological equipment used every day in hearing clinics and hospitals around the world. From our headquarters we sell to more than 100 countries through our own sales companies and external distributors, and we are part of the global hearing healthcare company Demant.
Ensure documentation of medical device products
We are on an exciting growth path and right now we are enhancing our capabilities in our Regulatory Compliance Team. If you are looking for a job in a top professional informal organization, this is the perfect place to do so!
Through your position you will have an immediate impact on regulatory compliance and future product development and launch. You will ensure our product compliance administration and maintenance of standard product documentation delivering valuable information to the regulatory department which ensures the right external product registration.
Ensuring new standards and recertification
As a team member in the compliance team, you will also be involved in regulatory surveillance and safety related risk analysis ensuring new standards and recertification are handled and new standards implemented in our knowledge base.
Working side-by-side with our developers and regulatory compliance team members, you will be responsible for and delivering:
Furthermore, the job is also to continuously improve our compliance process and following up on the latest new requirements.
Your contribution
Using your solid knowledge about product documentation, and requirements in the different markets you cooperate with project teams ensuring a smooth compliance process in line with the overall project plans.
We are looking for a candidate with a proven track record of regulatory compliance from a similar position which has involved documentation of electrotechnical, wireless products.
Being able to succeed, you should be familiar with regulations and processes for electrotechnical products such as risk analysis and familiar with international standards for medical devices
As a person it is crucial that you are diplomatic and able to coordinate the activities of the people around you. Ensuring structure and being systematic of course comes natural to you. Finally, you care about the details, and you have a "can-do" attitude.
Join our fantastic compliance department in Global Quality
You will be placed at our Interacoustics headquarters in Middelfart which is just one of many global brands that you will be working with. The other brands are placed in the UK, USA, and Germany.
At Interacoustics you meet all R&D disciplines under one roof. The compliance team is part of the quality organization and works closely with the development teams in R&D. Global Quality consist of 16 colleagues in total. Joining the compliance department, you will be part of a team of 4 people and on a daily basis, you will be reporting to our Compliance Manager.
We are based in a modern and open building where flexible work environment, knowledge-sharing and mutual professional respect making it fun and meaningful to be here. We all share the passion and the strong will to deliver premium quality in everything we do.
Do you want to join the team or learn more about the position?
Then send your CV and cover letter as soon as possible.
For more information about the position please contact Allan KARSBERG from KARSBERG Recruitment & Headhunting at +45 2113 2169.
We look forward to hearing from you.
Information og data
Denne ledige stilling har jobtypen "Bygningsarbejder", og befinder sig i kategorien "Industri, håndværk og teknik".
Arbejdsstedet er beliggende i Hele Danmark
Jobbet er oprettet på vores service den 8.9.2021, 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.
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