Senior Project Engineer
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Søborg
Senior Project Engineer – Cleaning SME
Do you want to be a part of an engineering project team in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!
You will become responsible for specifying and implementing Cleaning Equipment for our automation projects
We are expanding our production capability in site Søborg as we are approaching new markets with our products. To succeed with this, we are looking for a new colleague to join our department of Technology Innovation, Internal Engineering.
As our new Senior Project Engineer, you will be responsible for cleaning validation of new equipment and maintaining current validations in collaboration with Process Support. Further, you will perform project work for developing and specifying new filling production equipment – both for development purposes and capacity expansion of SURGIFLO®. Here you will be responsible for developing equipment specifications and production equipment to produce within these specifications. You will join a team of project engineers responsible for development of all internal processes and equipment in site Søborg, for the manufacturing of SURGIFLO® and other products.
In collaboration with stakeholders such as team members from Product Innovation and Process Support, you will prepare user requirement specifications, development studies, validation plans, and other documentation needed to ensure that we have effective processes, equipment, and high-quality products. Success in this role will require a structured and data-based approach, where you ensure and verify the correct documentation, and process impact.
A lot of your work will include close cooperation with both our external machine builders, manufacturing partners and internal stakeholders like Product Innovation, Quality Assurance and Manufacturing.
About you
As a person, you are a team player, and you are skilled in keeping an overview of your tasks. You are quality minded, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments. You thrive in a high pace environment.
You have a solid data-based approach to your work, and you understand the importance of documentation and processes. At the same time, you thrive when interacting with a range of different people. You have the skills to communicate and convey technical matters into more tangible formulations. Your language proficiency in both written and spoken English is at a professional level as many of your tasks will be executed in collaboration with English speaking colleagues.
Qualifications
Ideally, you hold an Engineering degree or similar and experience with specifying automated manufacturing equipment for manufacturing of medical devices (not a requirement).
Other relevant qualifications are:
We offer a truly purpose driven workplace where you can have real impact
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV latest at 23/04-2025. We will process the applications as we receive them.
We look forward to hearing from you.
Read more about us here
Do you want to be a part of an engineering project team in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Every 2nd second, Ferrosan Medical Devices’ products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team!
You will become responsible for specifying and implementing Cleaning Equipment for our automation projects
We are expanding our production capability in site Søborg as we are approaching new markets with our products. To succeed with this, we are looking for a new colleague to join our department of Technology Innovation, Internal Engineering.
As our new Senior Project Engineer, you will be responsible for cleaning validation of new equipment and maintaining current validations in collaboration with Process Support. Further, you will perform project work for developing and specifying new filling production equipment – both for development purposes and capacity expansion of SURGIFLO®. Here you will be responsible for developing equipment specifications and production equipment to produce within these specifications. You will join a team of project engineers responsible for development of all internal processes and equipment in site Søborg, for the manufacturing of SURGIFLO® and other products.
In collaboration with stakeholders such as team members from Product Innovation and Process Support, you will prepare user requirement specifications, development studies, validation plans, and other documentation needed to ensure that we have effective processes, equipment, and high-quality products. Success in this role will require a structured and data-based approach, where you ensure and verify the correct documentation, and process impact.
A lot of your work will include close cooperation with both our external machine builders, manufacturing partners and internal stakeholders like Product Innovation, Quality Assurance and Manufacturing.
About you
As a person, you are a team player, and you are skilled in keeping an overview of your tasks. You are quality minded, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments. You thrive in a high pace environment.
You have a solid data-based approach to your work, and you understand the importance of documentation and processes. At the same time, you thrive when interacting with a range of different people. You have the skills to communicate and convey technical matters into more tangible formulations. Your language proficiency in both written and spoken English is at a professional level as many of your tasks will be executed in collaboration with English speaking colleagues.
Qualifications
Ideally, you hold an Engineering degree or similar and experience with specifying automated manufacturing equipment for manufacturing of medical devices (not a requirement).
Other relevant qualifications are:
- Experience with cleaning validation
- Experience with specifying and qualifying equipment medical device or pharmaceutical production.
- Experience with specifying manufacturing equipment for other industries; food, automotive/other.
- Experience with and understanding of GMP, process risk management, validation, and qualification of production processes.
- Experience with the design control disciplines.
We offer a truly purpose driven workplace where you can have real impact
We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun 😊
Some of the facts and a little piece of history
Ferrosan Medical Devices develops and produces a portfolio of medical devices used in surgical care. Our portfolio consists of various hemostatic products to minimize bleeding challenges in surgery and electromechanical medical devices to perform breast biopsies. We are an international company with products registered in more than 100 countries. Our products are marketed in collaboration with global medtech partners. New ideas are developed and matured from the first thought to finished implementation in production. And we manage the business with an uncompromising focus on quality based on current GMP requirements.
Want to join our team?
Send your application along with your CV latest at 23/04-2025. We will process the applications as we receive them.
We look forward to hearing from you.
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 3.3.2025, 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.
- 02.04.2025
- IT-chef
- Søborg
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