Process Development Engineer
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 and Pharmaceutical organization, based in Noord-Brabant Netherlands.
Our client is a professional Medical Devices organization, based in Noord-Brabant Netherlands.
is a highly innovative company, with a unique product soon to enter the market.
ROLE DESCRIPTION
The products of the client are almost ready to enter the market. The organisation is switching from a R&D company to a manufacturing company. You will be helping the company to get its Manufacturing Process mapped and improved. You will improve the quality of the existing processes, and take the lead in improvement projects. After writing the processes, you will take the lead together with colleagues to execute process validations. In the role of Process Development Engineer you support also the production team and will be the point of contact for trouble shooting and root cause analysis.
RESPONSIBILITIES
- Improving Manufacturing processes
- Validation of processes
- Leading process projects
- Support of production team
- Upscaling of production and manufacturing processes
REQUIREMENTS
- Minimum of 4 years of experience in initiating, validating and improving of manufacturing processes in a fast paced environment
- Experience in highly regulated environment (Med Dev / Pharma / Chemie )
- Masters degree in Biomedical Engineering
- Smart, Systematic and Pragmatic attitude/approach - can do mentality
- Project Management, process validation, six sigma
- Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
