Ferrosan - Senior Project Engineer
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 next generation manufacturing equipment for internal paste filling processes
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 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 filling, assembly, or packaging of pharmaceutical products.
- 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.
