Quality Assurance Manager Ophthalmology
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 active in the ophthalmology branch of the Medical Devices sector. This organisation is well represented on both national and international level. They built their own brand but also offer products from private labels. This organisation is driven by collaboration of their various departments, who all work together to create a better and innovative brand.
ROLE DESCRIPTION
QA is a big deal within this organisation, therefore as manager you will carry out a main responsibility. The major focus is on the application of quality aspects and requirements of their products. Your team contains 10 members which are divided in QC and QA role. You will assess and improve the Quality Management System in assistance of your team. You are key in distribution of knowledge among your team, other departments and involved external parties. This project lasts at least for a year, with possibility for extension for another year.
RESPONSIBILITIES
Your overall responsibilities contain primarily over viewing the QMS and all involved regulations, in which you support your team to address new opportunities and build on better systems. Furthermore you will responsible for:
• Control and overview of legislation and regulatory documentation
• Creating additional value for the organsiation by bringing in your knowledge and experience regarding Quality Management System
• Directly reporting to the directors
• Interaction and maintenance of relationships among various stakeholders
• Application and creation of strategies concerning changes in regulations
REQUIREMENTS
• Master in Life Sciences
• 5 years of experience in QA role within Medical Devices industry
• 2 years of experience within ophthalmology branch
• Excellent communication skills both in Dutch and English
• Problem solving and analytical skills
• Mentoring and coaching ability
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.
