Quality Process Expert Consultant
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 Noord-Brabant Netherlands.
Worldwide key player within the Medical Devices industry with a broad and competitive portfolio of devices.
ROLE DESCRIPTION
The Quality Process Expert Consultant will contribute to improve the efficiency through the harmonization of the Quality Management System.
In this role, the Quality Consultant will intensively interact with multiple internal departments: design control, R&D, manufacturing, marketing, sales, procurement, distribution, PMS... and other external stakeholders.
Additional information
- Type of contract: temporary via payroll or freelance
- Duration: 6 months - 1 year (approx.)
- Starting date: 1st of February
- Location: 50% on site, 50% home-based
RESPONSIBILITIES
- Harmonization of different business processes into a solid QMS
- Ensure regulatory compliance
- Increase efficiency and optimization of the Quality Management System
- Act as Quality Business Process Expert in the Deployment Programs
- Offer Quality support to process modelling teams
REQUIREMENTS
- (at least) Bachelor degree in a technical or scientific discipline
- +10 years of experience in Quality within Medical Devices
- Proven track-record improving efficiency and optimizing processes (deployment)
- Good understanding of life-cycle and meaning in different fields (design, R&D, sales, distribution, marketing, PMS...)
- Expert in worldwide regulations: ISO 13485, FDA, JPAL, China regulations...
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.