Quality Control & Regulatory Affairs associate

SIRE Life Sciences® - More jobs by this advertiser
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Medical Devices organisation, based in Limburg Netherlands.

The Company

This organisation develops wound care products made from natural ingredients sold worldwide. They focus on innovation and creation of a broad international platform. They are exploring their position in the market and are aiming to increase their market share, therefore there are looking for new employees.

Role Description

You will become part of a dynamic and innovative business setting, that prioritises to protect the environment and nature. In your role as Quality Control and Regulatory Affairs officer you will be responsible for the launch of new products. Furthermore, you will be involved with the Quality Management System and ISO standards. Additionally, you are involved with required legislation and documentation. You will be reporting directly to the operation manager. This project is set for 6 months with possibility for extension to 9 months.

Responsibilities

• Maintenance of the Quality Management System and identifying points of improvements
• Controlling and adjustments regarding international legislation and regulations among which the CE-marking standards
• Responsible for product launch and compliant product specifications
• Follower of the latest developments and changes within international and European legislation and Quality standards

Requirements

• Bachelor of Sciences
• Minimal 4 years of experience in the Medical Devices industry
• Minimal 2 years of experience in Quality Control roles
• Excellent knowledge of European regulations
• Practical experience with ISO 13485 and Good Manufacturing Practice
• Team player, yet individual operator
• Pro-active attitude with eye for detail
• Strong communicator
• 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.


SIRE Life Sciences®


Amsterdam, (Netherlands)

Phone: +31 (0)20 658 9800
Web: http://sire-search.com

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Company Profile

6 February 2019
Location: Netherlands Limburg Limburg
Salary: Competitive Salary
Work type:
Temporary/Contract
Sector:
Life Sciences
Profession:
Testing and Quality Assurance

This career opportunity is no longer open.
Please search for current vacancies here.


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