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 Medical Devices organization, based in Gelderland Netherlands.
They are a global organisations that is pushing the limits to what Technology, services and therapies can do. They challenge themselves and their employees to make a better tomorrow for everybody.
ROLE DESCRIPTION
They are looking for a new Quality Assurance Officer because of a missing employee who is with maternity leave. Therefore you will be strengthening the team on a project basis for half a year. Depending the performances and team and your wishes your contract can be extended. You will work with the team and support with the implementations of quality requirements regarding the devices of the company.
RESPONSIBILITIES
Your main tasks will be to actively manage and monitor preventive or corrective actions within the QMS and report this to your superior the QA manager. Other responsibilities will be:
• You will support QA aspects regarding quality and regulatory EMEA standards concerning devices who go abroad or even outside Europe
• You will conduct projects and processes regarding quality improvement
• Conducting internal audits to assess trends and opportunities to improve the quality of the processes
• You will be responsible of complain handling and coordinating the follow-up
REQUIREMENTS
• Bachelor degree in Engineering, Health or a similar degree
• 1 to 5 years’ experience in the medical device industry or another highly regulated environment
• Experience in the implementation and improvement of Quality Systems
• Excellent in English language both writing and speaking
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.
