Quality Assurance Coordinator
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.
They are an innovative technology company focusing on high-tech electronics, software and medical devices as a manufacturer of own products and outsource manufacturer. They are looking for a Quality Assurance coordinator to take responsibility in the Quality activities and support the different sites of the company.
ROLE DESCRIPTION
As the QA Coordinator you will be part of the team and contribute to the Quality Management System of the organisation. Here you will support different entities and develop/improve their local QMS. The environment will be dynamic and diverse from software and electronics to mechatronics with a Medical Device focus. Traveling will be a part of the position where you will commute between different sites within North Brabant.
RESPONSIBILITIES
The main tasks and responsibilities you will fulfill:
• Monitor and support the development and improvement of the (local) QMS
• Stimulate activities and mindset to improve quality, change management
• Monitor relevant regulatory affairs and changes in law
• Coordinate Quality activities and set in motion improvement projects
REQUIREMENTS
• Experience with ISO 13485:2003 and ISO 9001:2008, as a preference an auditor
• Knowledge of ISO 13485:2016 and ISO 9001:2015
• Plus 10 years of experience with knowledge in development and production of software and mechatronics, multilayered QMS, change management
• Broad organisational scope
• Lean and Mean Attitude
• Fluent in English and Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.
