Senior Project Manager for Medical Device Development
Do you want to design safe and reliable medical devices, helping patients to better treatment? Are you ready to lead complex development projects, delivering on time to customer satisfaction? Do you want to cooperate with highly skilled colleagues to bring new products to market in a fast growing and successful global company?
Then you may be what we are looking for in Phillips-Medisize’s Global Innovation & Development Center in Virum (Greater Copenhagen).
What You Will Do In Your Role
You will be leading cross functional development projects, delivering new medical devices to our global pharma clients with focus on customer requirements and business value.
As Senior Project Manager you are part of scoping the projects in the contractual agreements and you establish and align deliveries with the client throughout the project from start to production transfer or delivered solution. Your key tasks are to ensure effective delivery of the right solutions in the right quality, motivate your team and perform overall scope management of your project.
Planning, budgeting and continuous progress is your responsibility, and you are one point of contact towards the client. You ensure communication to both internal and external stakeholders, and cooperation with e.g. regulatory authorities, suppliers and testing laboratories is an important part of the job.
We work in an international and creative environment and you will collaborate closely with colleagues from the global Phillips-Medisize organization, especially with our development team in Struer and with our production sites in Europe, North America and Asia.
In this position you have great opportunities to influence the products we develop and our way of working, contributing to our growing business.
The Experience You Will Bring
You have a Master or Bachelor´s degree in engineering, a proven track record of 5+ years of successful project management preferably from the Medical Device industry, and knowledge within Medical Device regulations and standards (21CFR, ISO13485, ISO14971). You are experienced in driving projects from concept to industrialization phase, and your commercial understanding is excellent and so is your ability to transfer this to project execution. Furthermore, you are skilled in project management tools as JIRA or MS project.
You combine strong leadership skills with openness to input from colleagues, work to get the best out of your team and thrive with solving complex challenges. You communicate effectively on different organizational levels and with both technical and non-technical stakeholders and are fluent in English speaking and writing.