SIRE Life Sciences®

Quality Coordinator

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 Utrecht Netherlands.

They are a global Medical Device company specialised in manufacturing devices and technologies used in hospitals and medical rooms.

ROLE DESCRIPTION

They are looking for an extra supervisor to join the team that is rapidly expanding at their current headquarters located here in the Netherlands. In this role you will support the production of all medical devices by ensuring all final products meet the requirements and standards that are asked of them. The role of coordinator will supervise a team of Quality specialists and ensure that all processes are performed according to all current and future standards and requirements.

RESPONSIBILITIES

As the new Quality Assurance coordinator you will supervise a team that will be responsible for the quality of all final products. Next to that you will have multiple responsibilities:
• Investigate and assess non-conformities
• Assess all test results regarding all quality processes and ensure they are aligned with quality requirements
• Responsible for all procedures and quality instructions
• Control and assess quality control testing
• Participate in hiring process for new team members

REQUIREMENTS

• At least a bachelor degree
• Minimum of three years in supervising or team leading
• Experience with quality systems in a highly regulated environment (Pharma/medical devices)
• Fluent in both Dutch an English is a must
• Experience with ISO 13485 and FDA
• Strong communication skills in multiple levels of a organisations

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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