Freelance Quality Assurance Specialist
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-Holland Netherlands.
They are an international supplier of various medical solutions on the healthcare market.
ROLE DESCRIPTION
As a quality assurance specialist you will secure that the quality systems and the products are in compliance with the international regulatory standards. You will be contacting multidisciplinary teams from different departments in the company. We are looking for an independent, dynamic and professional freelancer, who will help professionalize the Quality Management System and train your colleagues.
This project will be full time for 6 months, on site.
RESPONSIBILITIES
You will ensure compliance to all regulations, quality systems and ISO 13485 norms. As well as internal procedures by proactively interpreting regulatory and quality requirements and determining way of working.
• Continuously improving of the quality management system in the company
• Secure the functioning of the self-inspection systems
REQUIREMENTS
• BSc or MSc in Life Science related fields
• +-3 years of experience in Quality Assurance in the medical device industry
• Knowledge of the medical devices regularity and quality standards (GMP guidelines, ISO 13485, 21CFR820, European Directive 2004/23)
• Expert in internal and external audits and quality systems (i.e. change control, CAPA, deviations, etc.)
• Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rombout van Rees.
