Project Engineer with medical device experience
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Søborg
Do you want to contribute to developing and optimising world-class products used in vital operations? And you motivated by becoming part of the whole development process from idea and design to development and validation?
At Ferrosan Medical Devices, we are looking for a project engineer who will gain a big degree of responsibility in our device development projects.
Join our Technology Innovation team
We develop and produce a portfolio of hemostatic products to minimise bleeding challenges in surgeries. Our products are registered as medical devices and sold internationally to more than 100 countries. All main functions in the company, including our production facilities, are based in Soeborg, Denmark, so everyone sits door to door with easy access to each other.
You will be joining our Technology Innovation team, where we are 12-15 engineers and pharmacists who participate in development projects for new devices. Our role is to ensure that the production process is validated, qualified and optimised, whether it takes place internally or externally. We work within a range of areas, including the moulding process, blister packs and sterilisation.
Contribute to design, validation and documentation
As our new project engineer, you will be working in our development project teams. Our teams vary a lot in size and duration, including anything from 4 to 15 people and lasting from a couple of months up to a couple of years. You will be one of our design control and/or validation specialists, and your focus will be on ensuring important documentation, including e.g. risk assessments, validation plans and specifications related to the development of new products.
Based on your experience and wishes, you will be covering the following areas together with your team – if you need to update your knowledge on some areas, we will make room and find resources to do so.
Specifically, you will:
• Be our design control specialist and prepare relevant documentation
• Be responsible for validation and qualification from FAT to PQ
• Participate in development projects and contribute to detailed design of products, packaging, etc.
• Cooperate with external suppliers and CMO´s within plastics moulding and packaging
“In this role, you will get a wide range of responsibility and be part of our device development projects from start to finish, bringing you close to the end products and giving you a big degree of influence,” says Director Lotte Juul Foghsgaard.
Project experience within a GMP-regulated environment
With a good amount of professional and personal stamina, you thrive in a busy environment where you can not always find detailed manuals for everything. Like us, you handle things through dialogue, and you trust that your colleagues make the right decisions.
You are motivated by taking an active role in the production process, from idea to validation, and you find it exciting being close to the products. Also, you know how to interact and share knowledge with a lot of different people in different functions which is vital in a small company – both internally and externally.
Furthermore, we imagine that you have:
• A relevant degree within e.g. engineering or pharma
• Experience working with projects in a GMP-regulated environment
• Good experience with development projects that have documentation requirements
Want to join the team?
Send Your application along with your CV via the link below as soon as possible. We will process the applications as we receive them.
Questions? Do not hesitate to contact director Lotte Juul Foghsgaard on +45 2089 8046.
We look forward to hearing from you.
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
At Ferrosan Medical Devices, we are looking for a project engineer who will gain a big degree of responsibility in our device development projects.
Join our Technology Innovation team
We develop and produce a portfolio of hemostatic products to minimise bleeding challenges in surgeries. Our products are registered as medical devices and sold internationally to more than 100 countries. All main functions in the company, including our production facilities, are based in Soeborg, Denmark, so everyone sits door to door with easy access to each other.
You will be joining our Technology Innovation team, where we are 12-15 engineers and pharmacists who participate in development projects for new devices. Our role is to ensure that the production process is validated, qualified and optimised, whether it takes place internally or externally. We work within a range of areas, including the moulding process, blister packs and sterilisation.
Contribute to design, validation and documentation
As our new project engineer, you will be working in our development project teams. Our teams vary a lot in size and duration, including anything from 4 to 15 people and lasting from a couple of months up to a couple of years. You will be one of our design control and/or validation specialists, and your focus will be on ensuring important documentation, including e.g. risk assessments, validation plans and specifications related to the development of new products.
Based on your experience and wishes, you will be covering the following areas together with your team – if you need to update your knowledge on some areas, we will make room and find resources to do so.
Specifically, you will:
• Be our design control specialist and prepare relevant documentation
• Be responsible for validation and qualification from FAT to PQ
• Participate in development projects and contribute to detailed design of products, packaging, etc.
• Cooperate with external suppliers and CMO´s within plastics moulding and packaging
“In this role, you will get a wide range of responsibility and be part of our device development projects from start to finish, bringing you close to the end products and giving you a big degree of influence,” says Director Lotte Juul Foghsgaard.
Project experience within a GMP-regulated environment
With a good amount of professional and personal stamina, you thrive in a busy environment where you can not always find detailed manuals for everything. Like us, you handle things through dialogue, and you trust that your colleagues make the right decisions.
You are motivated by taking an active role in the production process, from idea to validation, and you find it exciting being close to the products. Also, you know how to interact and share knowledge with a lot of different people in different functions which is vital in a small company – both internally and externally.
Furthermore, we imagine that you have:
• A relevant degree within e.g. engineering or pharma
• Experience working with projects in a GMP-regulated environment
• Good experience with development projects that have documentation requirements
Want to join the team?
Send Your application along with your CV via the link below as soon as possible. We will process the applications as we receive them.
Questions? Do not hesitate to contact director Lotte Juul Foghsgaard on +45 2089 8046.
We look forward to hearing from you.
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 "IT-chef", og befinder sig i kategorien "Informationsteknologi".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 21.12.2021, 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.
- IT-chef
- Søborg
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