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 Utrecht Netherlands.
They are a dynamic organization and besides producing their own devices they consult and support as well. They are European wide active and looking for a fulltime Manager in Quality Assurance.
ROLE DESCRIPTION
You will be responsible for company quality and compliancy with all regulations concerning quality affairs. This means that you will focus on developing a yearly strategy for assessing and implementing quality updates and improvements. As the new QA Manager you will follow this plan and assess results according to the company’s plan and targets. Beside you will conduct and lead the audits conform ISO 9001:2015 and ISO 13485:2016.
RESPONSIBILITIES
• Assess performances of Quality employees and supervise in trainings
• Internal and External Audits
• End responsible for complain handling, Post Market Surveillance
• Translating the build yearly strategy to separate department plans and monthly plans
• Being up to date with all changes in regulations and quality affairs and implement changes in the Quality strategy
• Serve as single point of contact in quality towards supervisors and plan periodic meetings to report results, possible non-conformities, up-dates, improvements, etc..
• As the new manager you will be responsible as well for the educational division of the company where new employees will be trained regarding all quality & regulatory affairs
REQUIREMENTS
• Relevant working experience with a Medical Device background and environment
• A minimum of two years of management experience.
• Strong in communication and motivation
• Working knowledge of ISO 13485 & 9001
• Fluent in both 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.
