Quality Assurance 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 Noord-Brabant Netherlands.
They are a low volume, high mix manufacturer of functional critical Components and Systems for the Aerospace and Defense, the Semiconductor, Medical & Diagnostic and Industrial Automation industries.
ROLE DESCRIPTION
For their Medical Devices department, they are looking for a Quality assurance manager. You will drive and support Quality and regulatory to assure that their product comply to the quality management system. As well as creating quality function deliverables for the quality management system in projects, in life cycle management and in post market surveillance at their development site.
RESPONSIBILITIES
You will be deploying, securing and monitoring the quality policies. Supporting and advising at entering new and improved products into the market. Assure that they comply with applicable international regulations.
- Implementing and monitoring internal and supplier audits, Independently and in teams.
- You will Instruct, support and facilitate project teams with regards to the quality management system
- Ensure compliance to quality system requirements, regulations and standards in designated area of responsibility
- Coordination and follow up of extern audits
REQUIREMENTS
- BSc/MSc Degree, with a technical background by preference
- Minimum of +-5 years of relevant working experience
- Certified lead auditor ISO13485
- Knowledge of relevant laws and regulations in Medical Devices
- The ability to develop and coach teams
- Strong communicative skills
- Fluent in Dutch and English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact .
