Quality Assurance Manager Overijssel
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.
This organisation is recognized as international market leader. They are both manufacturers and distributors of medical devices and related technologies. Their specialty lies in urology and gastroenterology. Their products are intended to improve and make lives of patients more convenient.
ROLE DESCRIPTION
As a Quality Assurance manager you are responsible for a team consisting out of several QA professionals. You will direct your team in maintaining and improving the QMS, required documentation and quality control. Next to that, you will receive the responsibility to gain insight into lack of knowledge and as a result you will develop trainings and additional tools. You are the key person to develop relationships with internal and external stakeholders, among which you collaborate closely with the Regulatory Affairs team and international QA teams. This role is an interim position for 8 months with possibility for extension.
RESPONSIBILITIES
• Collaborate closely with clients and relevant stakeholders to gain insight into issues and points of improvement
• Taking the lead in audits and related processes, from the beginning to the end
• Improve and maintain the Quality Management System supported by team members
• Overview required documentation and keep on track of latest developments on quality and regulatory affairs
• Key representative for various stakeholders across the organisation
• Giving permission for suppliers and distributors regarding the Quality of new products and their specification
REQUIREMENTS
• Bachelor of science
• 7 years of experience within the Medical Devices industry
• 6 years of experience in a QA role
• Excellent knowledge of ISO13485 and relevant procedures
• Proven experience in handling complaints with involved parties
• Excellent leadership and organizational skills
• Fluent in English, and understanding of Dutch
• Strong strategic and analytical skills
• Team player, yet ability to make decisions
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.
