Quality Assurance Officer Ophthamology
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 Zuid-Holland Netherlands.
This client is a global leader in the ophthalmology sector and aims to work directly with hospitals. This close collaboration enables the company to evaluate and improve their products immediately in need of their clients. This guarantees rapid development and high- quality products.
ROLE DESCRIPTION
There is nothing above quality within this organisation. In your role as quality associate, you have to responsibility to control and review the documentation which is required for their products. This also contains the documentation of new products and requires strict assessment before these products are launched internationally. You will have a supportive role in which you directly report to the Quality Assurance manager. In addition, you will interact on a daily basis with the product management department. This job will last for 4 months and can be extended with 4 months on top.
RESPONSIBILITIES
One task within your daily routine is to constantly review and maintain product standards and regulations in order to proceed with the development of these products for both the national and international market. Furthermore your responsibility lies in:
• Monitoring and identifying changes within the production stage which should all be in line with the Quality Management Systems
• Offering guidance in internal and external audits, from the beginning to the end
• Offering support to the project manager by assisting in over viewing the process and planning
• Being responsible for maintenance and assessment of all product documentation which must be clearly in line with required regulations and legislation
• Maintain the relationship with the project management department and ensure close interaction
REQUIREMENTS
• Master degree in pharmacy
• 3 years of experience within Medical Devices industry
• Excellent knowledge of European and Global Medical regulations
• 1 year of experience in QA of ophthalmology
• Fluency in Dutch and English
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.
