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Quality Officer/Manager

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Quality Officer/Manager

Location: Netherlands

SIRE 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 a young international medical device company specialised in Ophthalmic devices and medical solutions

ROLE DESCRIPTION

As the new Quality Assurance engineer your daily tasks will involve all ensuring that each product is manufactured according to all new requirements, company regulations policies and Market Authorisations. You will work in a small company where you will be responsible for the QA activities and compliance.

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.

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SIRE Life Sciences®

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