Project Engineer
at Ferrosan Medical Devices
2860 Søborg, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 Sep, 2024 | Not Specified | 27 Jun, 2024 | N/A | Validation,Gmp,Medical Devices,Production Processes,Pharmaceutical Industry,Manufacturing | No | No |
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Description:
Project Engineer in medical devices
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!
QUALIFICATIONS
Ideally you hold an Engineering degree or similar and experience with specifying automated manufacturing equipment for manufacturing of medical devices.
Other relevant qualifications are:
- Experience within the medical devices or pharmaceutical industry.
- Experience with specifying manufacturing equipment for other industries; food, automotive.
- Experience with and understanding of GMP, process risk management, validation, qualification of production processes.
- Experience with the design control disciplines.
- You can be newly educated with relevant experience from your student assistant job.
Responsibilities:
YOU WILL BECOME RESPONSIBLE FOR SPECIFYING AND IMPLEMENTING NEXT GENERATION MANUFACTURING EQUIPMENT FOR CAPACITY EXPANSION PROJECTS
We are expanding our production capability in site Søborg as we are approaching new markets with our products. For that we need a new colleague to join our Technology Innovation, Internal Engineering, department.
As our new project engineer, you will be responsible for specifying new equipment for development projects and capacity expansion. You will be a work package owner and will be responsible for planning the course of 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.
Success in this role will require a data-based approach, where you ensure and verify the correct documentation, and process impact.
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.
A lot of your work will include close cooperation with both our external machine builders, manufacturing partners and internal stakeholders like e.g., Product Innovation, Quality Assurance and Manufacturing.
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!
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Engineering Design / R&D
Clinical Pharmacy
Graduate
Engineering
Proficient
1
2860 Søborg, Denmark