Freelance Quality Assurance Officer
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 Clinical Research and Medical Devices organization, based in Netherlands.
This business is booming at the moment. They offer a set of services that focus especially on clinical research, studies and trials within the Medical Devices sector. They perform studies all over the world deviating from cardiovascular surgery to radiology. They have phenomenal expertise and will always live up to their high-set standards.
ROLE DESCRIPTION
As a QA officer, you will become part of the QA team. You will have a supportive role in which you evaluate processes and report critical points of improvement, directly to the QA manager. The most important responsibility within your daily routine is to assess the performance and maintain the Quality Management System. Next to that, you are in charge of the control of all regulatory and quality assurance documentation. This project is set for a year.
RESPONSIBILITIES
• A critical role within the development of quality projects
• Offer guidance in the entire audit process from the beginning to the end
• Maintain and improve the organisation’s standard operating procedures
• Create and assess an overview of their Key Performance Indicators
• Order all documentation and create a strategic logic organization of documentation and files
• Development practical trainings and records for internal and external stakeholders
REQUIREMENTS
• Bachelor Degree in Life Sciences
• Minimal 3 years of experience with QA in Medical Devices Branch
• Highly developed communication and interrelation skills
• Experience with ISO 9001 and ISO 13485
• Fluent English and Dutch
• Pro-active attitude with hands-on mentality
• A perfectionist
• Great feeling for logically organizing and planning
• Not afraid to be challenged
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.
