Labelling Specialist
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Søborg
Labelling Specialist
Do you want to help create and update medical device labels of a product portfolio that helps patients globally?
At Ferrosan Medical Devices, our Product Development department is continuously working to improve processes and adapt to new challenges – and we hope that you want to join us on this journey.
Join a highly professional team in Product Development, Biomaterials
Ferrosan Medical Devices develops haemostatic products that doctors in over 100 countries worldwide use to minimise bleeding during surgeries. Our products are quite literally vital.
Based out of our HQ in Søborg with 230 colleagues, you will be joining our Product Development department of 12 professionals, placed under our New Business Development. Here, we are experienced and diverse in both skill sets and backgrounds. And as a team, we work hard and with dedication to deliver holistic support as we:
- Define technical requirements for the product documentation in accordance with design control
- Handle the design control, biosafety and product labelling as we ensure the preparation of design input and outputs as well as design verification and validation
- Prepare the necessary technical evidence, rationales and data to ensure that the product design meets the required functionality, efficiency and safety of our Class III products
Translate and update the labelling of our product portfolio
As our new labelling specialist, you will be responsible for creating and updating medical device labelling for our haemostatic product portfolio. Doing so, you will be part of a development team where you will manage many different inputs and translate them into compliant product labelling.
You will work in cross-functional teams to ensure that we meet the product labelling requirements. This means that you will be involved in product development projects where you will create printed labels and package artwork for new products, collaborating closely with production and various external partners.
Moreover, you will be involved in life cycle management tasks and projects, where you will ensure that our product labelling on our legacy products is compliant.
Specifically, your tasks will include that you:
- Translate product labelling requirements into release labels and package artwork according to internal procedures, product requirements and company branding guidelines while being compliant with the global standards
- Ensure ongoing updates of product labelling to meet emerging regulatory requirements
- Handle ongoing updates of labelling processes according to regulatory requirements, quality system or branding policies and strategies
“You will be part of a truly dedicated team where we collaborate closely. And you will also get to grasp and handle many great ideas which you build your artwork on,” explains Senior Manager, Product Development, Biomaterials, Mette Krog Keller.
Self-driven and structured with a relevant background
As you will be interfacing with colleagues from all levels and functions in the organisation and with external partners, you must be a competent communicator for whom stakeholder management comes naturally.
Furthermore, we imagine that you:
- Have a relevant educational background and experience from a similar role in the medical or pharmaceutical industry
- Are familiar with medical device regulations as well as a basic understanding of design control – or the willingness to learn it
- Understand the UDI regulation and are able to translate this into product labelling requirements
- Have solid knowledge of Adobe Illustrator and/or InDesign
- Have experience with ISO 15223 and ISO 20417
- Speak and write Danish and English fluently
Interested?
Then click the link below and submit your application and CV. We will be evaluating candidates continuously throughout the process, so make sure to apply as soon as possible.
If you have any questions about your new job, feel free to reach out to Peoplement Anne Borgen 6169 0101 or e-mail [email protected].
About us
Since 1947, we have developed and manufactured haemostatic products, used by healthcare professionals to stop bleeding during surgical operations. Our focus is to develop solutions to clinical problems within biosurgery – and to provide healthcare professionals with new innovative therapeutic alternatives that make a positive difference to them and ultimately improve patient outcomes. 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 1.12.2021, 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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