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 Overijssel Netherlands.
They are a Dutch company which have products that is used throughout the world and has a still growing reputations concerning the Medical Devices they produce and the expertise they deliver with that.
ROLE DESCRIPTION
As the company is still growing they need a Quality Assurance Manager to take lead over a team of 6 specialists that will be specialized in different disciplines. Besides your responsibilities you will manage this team, take reviews, support development plans and drive teamwork between the teams as the Quality contact point. You will also serve as EMEA contact point and if needed would go on business trips to clients (expected once every three to five months).
RESPONSIBILITIES
Your main responsibilities will involve product and process Risk & Quality Management, improving the QMS to current standards and achieve expected results with the company strategy that you will manage with your team. Other responsibilities would be:
• Complaint review
• Conduct validations processes
• Audits both internal and external
• Design controls and Design Transfer, Design Changes
• Analyze current processes and perform corrective/preventive actions concerning Quality
REQUIREMENTS
• Bachelor or Master degree
• At least 10 years ‘experience and preferably within the Medical Device Industry or any other Product environment
• Solid experience in auditing, preferable lead-auditor certified
• Experience in Change Management
• Proven management skills
• Strong Leadership and Influencing skills, the ability to inspire
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.
