Temprorary Medical Device project manager
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Zuid-Holland Netherlands.
This organisation is active in the ophthalmology sector. They focus on the development of highly innovative, technological instruments. This organisation is rapidly growing and maintaining a strong position on an international level.
ROLE DESCRIPTION
In your role as project manager you will coordinate the various projects within the organisation. You will create a planning, gain insights into the risks and you will monitor the budgets. You will be the key contact person when it comes to organizing and offering solutions. You have to direct and keep an overview of the projects. Additionally, you will be the contact person for suppliers, when they have issues or complaints. This project intends to last for 6 months and can be extended with 2 additional months.
RESPONSIBILITIES
Your focus on giving advice and support to all departments and teams. You will assist to create efficient and effective procedures to bring the projects to a good end. Furthermore, your responsibilities involve:
• Planning and organisation and coordinate the activities of medical projects
• Indication of the risks and creating solutions to avoid these risks
• Creating budget plans
• Controlling and overviewing the developments and progress of the projects
• Identifying and implementing points of improvements
• Making reports for the sales department, R&D department and CEO
• Evaluation of all projects and the collaboration among the departments
REQUIREMENTS
• Bachelor in Engineering
• Minimal 5 years of experience within the Medical devices industry
• Minimal 2 years of experience in an strictly regulated environment
• Broad knowledge of R&D, Regulatory Affairs and Quality Assurance within a Medical Device organisation
• Team player with extraordinary communication skills
• Fluency in English, and good understanding of the Dutch language
• Experience as auditor for both internal and external stakeholders
• Critical scope and excellent organisational skills
• Hands-on mentality
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.
