Project Engineer
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Søborg
Are you motivated to work with lifesaving products in a company where you get the chance to become a vital support to our value chain? And do you want to take part in developing our next generation manufacturing equipment?
Then join us at Ferrosan Medical Devices, where high ambitions, success and focus on quality goes hand in hand with job satisfaction, flexibility, and work-life balance.
Welcome to a specialised and innovative team
Ferrosan Medical Devices develops haemostatic products that are used worldwide to minimise bleeding during surgeries. Our products help save lives, and now you get to play an important part in the development of these products. Joining us at our HQ in Søborg, you will become an integral part of our Technology Innovation department, consisting of 17 highly specialised engineers and pharmacists.
Our responsibility is to transfer product requirements into specific equipment and process requirements. We ensure sourcing of equipment from suppliers and are responsible for specification, qualification, validation, process transfer and ramp-up/optimisation, whether it takes place internally or externally. We work within a range of areas, including the basic gelatine process, moulding of components, kitting, blister packaging, sterilisation, finished goods packaging etc.
Responsible for specifying next generation manufacturing equipment for development projects and capacity expansions
As our new project engineer, you will be responsible for specifying new equipment for development projects and capacity expansions. You will be work-package-owner and will be responsible for planning the course of the machine production together with the supplier of the equipment. In accordance with internal procedures, you will be responsible for preparing the process risk management, URS, validation plans, and the documentation needed to ensure we will have effective equipment producing safe and high quality products. Furthermore, you will provide support to the machine builders, and be the technical contact person on behalf of FeMD. Finally, you will be accountable for adhering to the schedule which you have aligned with the overall project manager. Success in this role will require a 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 production and other internal stakeholders like e.g., QA, QC.
”This is a chance to make an impact on our business – there is a lot of potential for you to make your mark on our future processes and workflows, based on a solid data foundation,” says Director of Technology Innovation, Jannik Dipo Knudsen.
An academic with good data and process skills
With a knack for having a solid data-based approach to your work, you understand the importance of documentation and processes – especially in a GMP-regulated environment. At the same time, you thrive when interacting with a range of different people. Additionally, you have the skills to communicate and convey technical matters into more tangible formulations. Additionally, 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.
As a person, you are skilled in keeping an overview of your tasks and handling a large amount of data and documents. You are quality-conscious, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments
Qualifications
Ideally you hold an Engineering degree or similar.
We furthermore imagine that you have:
Want to join the team?
Send your application along with your CV via the link below no later than 25 October 2022. We will process the applications as we receive them.
Questions? Do not hesitate to contact Director of Technology Innovation, Jannik Dipo Knudsen on +45 5213 2882.
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.
Then join us at Ferrosan Medical Devices, where high ambitions, success and focus on quality goes hand in hand with job satisfaction, flexibility, and work-life balance.
Welcome to a specialised and innovative team
Ferrosan Medical Devices develops haemostatic products that are used worldwide to minimise bleeding during surgeries. Our products help save lives, and now you get to play an important part in the development of these products. Joining us at our HQ in Søborg, you will become an integral part of our Technology Innovation department, consisting of 17 highly specialised engineers and pharmacists.
Our responsibility is to transfer product requirements into specific equipment and process requirements. We ensure sourcing of equipment from suppliers and are responsible for specification, qualification, validation, process transfer and ramp-up/optimisation, whether it takes place internally or externally. We work within a range of areas, including the basic gelatine process, moulding of components, kitting, blister packaging, sterilisation, finished goods packaging etc.
Responsible for specifying next generation manufacturing equipment for development projects and capacity expansions
As our new project engineer, you will be responsible for specifying new equipment for development projects and capacity expansions. You will be work-package-owner and will be responsible for planning the course of the machine production together with the supplier of the equipment. In accordance with internal procedures, you will be responsible for preparing the process risk management, URS, validation plans, and the documentation needed to ensure we will have effective equipment producing safe and high quality products. Furthermore, you will provide support to the machine builders, and be the technical contact person on behalf of FeMD. Finally, you will be accountable for adhering to the schedule which you have aligned with the overall project manager. Success in this role will require a 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 production and other internal stakeholders like e.g., QA, QC.
”This is a chance to make an impact on our business – there is a lot of potential for you to make your mark on our future processes and workflows, based on a solid data foundation,” says Director of Technology Innovation, Jannik Dipo Knudsen.
An academic with good data and process skills
With a knack for having a solid data-based approach to your work, you understand the importance of documentation and processes – especially in a GMP-regulated environment. At the same time, you thrive when interacting with a range of different people. Additionally, you have the skills to communicate and convey technical matters into more tangible formulations. Additionally, 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.
As a person, you are skilled in keeping an overview of your tasks and handling a large amount of data and documents. You are quality-conscious, and you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments
Qualifications
Ideally you hold an Engineering degree or similar.
We furthermore imagine that you have:
- Solid experience within the medical devices or pharmaceutical industry.
- Experience with and understanding of GMP, validation, qualification of production processes.
- Experience with the design control disciplines.
- Experience with and insight into data management and statistics.
Want to join the team?
Send your application along with your CV via the link below no later than 25 October 2022. We will process the applications as we receive them.
Questions? Do not hesitate to contact Director of Technology Innovation, Jannik Dipo Knudsen on +45 5213 2882.
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.
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 14.7.2022, 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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