Sr. R&D Scientist
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Søborg
Sr. R&D Scientist
Do you want to take on responsibility for coordinating, planning and documenting product performance requirements across a wide range of products that help 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 team, we work hard and with dedication to deliver holistic support as we:
Collaborate across functions as you coordinate and update product performance requirements
As our new R&D scientist, you will spend the majority of your time driving the delivery of high-quality technical documentation in alignment with the design control processes, regulatory legislation and standards across the company.
Doing so, you will collaborate with multiple colleagues and partners across Product Development, Regulatory Affairs as well as Quality & Production in assigned project teams.
You will be covering several aspects within the haemostatic product portfolio, though you will have your primary focus on product performance requirements. Moreover, you will also be supporting operational projects within the organisation.
Specifically, your tasks will include that you:
“You will be part of a truly dedicated team where we collaborate closely. And you will get to heighten the quality as you define the future standards of documentation,” explains Senior Manager, Product Development, Biomaterials, Mette Krog Keller.
Self-driven and structured with a solid scientific background
You are a self-driven scientist with an inherently problem-solving mindset. And as you will be interfacing with colleagues from all levels and functions in the organisation, you must be a competent communicator for whom stakeholder management comes naturally.
Furthermore, we imagine that you:
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.
Do you want to take on responsibility for coordinating, planning and documenting product performance requirements across a wide range of products that help 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 team, we work hard and with dedication to deliver holistic support as we:
- Take responsibility for generating and maintaining compliant technical documentation within product design, functionality, safety, effectiveness and labelling
- Set up product design requirements and define acceptance criteria for product performance and safety
- Create high-quality documentation within design control, supporting regulatory registrations
Collaborate across functions as you coordinate and update product performance requirements
As our new R&D scientist, you will spend the majority of your time driving the delivery of high-quality technical documentation in alignment with the design control processes, regulatory legislation and standards across the company.
Doing so, you will collaborate with multiple colleagues and partners across Product Development, Regulatory Affairs as well as Quality & Production in assigned project teams.
You will be covering several aspects within the haemostatic product portfolio, though you will have your primary focus on product performance requirements. Moreover, you will also be supporting operational projects within the organisation.
Specifically, your tasks will include that you:
- Take overall responsibility for planning, coordinating, documenting and executing performance studies, e.g. packaging performance testing and stability studies
- Write technical documentation together with the team, e.g. test protocols and reports, technical evaluations and regulatory rationales – with guidance from cross-functional partners
- Update product requirements and define acceptance criteria product performance and safety
- Revise and create material specifications
“You will be part of a truly dedicated team where we collaborate closely. And you will get to heighten the quality as you define the future standards of documentation,” explains Senior Manager, Product Development, Biomaterials, Mette Krog Keller.
Self-driven and structured with a solid scientific background
You are a self-driven scientist with an inherently problem-solving mindset. And as you will be interfacing with colleagues from all levels and functions in the organisation, you must be a competent communicator for whom stakeholder management comes naturally.
Furthermore, we imagine that you:
- Have a relevant scientific educational background
- Have experience from a similar role in the medical device, pharma, medico, or from other regulated industries
- Have experience with ISO 13485 and the MDR legislation
- Can show examples of experience with the generation of quality documentation within GDP and design control – from verification to design input and final design transfer
- Can plan and design performance studies that document the product integrity throughout the product lifecycle
- Take responsibility for driving and completing your tasks successfully
- 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 "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 2.12.2021, 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.
- Forsker
- Søborg
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