SIRE Life Sciences®

QA Specialist

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 Zuid-Holland Netherlands.

They are a global company with headquarters stationed in the Netherlands. They focus on Ophthalmic devices to enhance and provide eye surgery and solutions.

ROLE DESCRIPTION

As a quality assurance specialist you are responsible for implementing, safeguarding and monitoring our quality policy. You are also responsible for setting up, managing, maintaining and continuously improving the quality management system in accordance with the applicable international requirements for medical device manufacturers.

RESPONSIBILITIES

• Implement, safeguard and monitor the quality policy.
• Set up, manage, maintain and continuously improve the quality management system.
• Implementing applicable international requirements in the quality management system.
• Advising and supporting the introduction of new and changed products, working methods and procedures and ensuring that these comply with the applicable international regulations.
• Training and coaching colleagues.
• Coordinate and follow up the management review.
• Adviseren en begeleiden van uitbestedingsprojecten.
• Opstellen, beoordelen en vrijgeven van diverse documenten.
• Initiëren en bewaken voortgang van corrigerende en preventieve maatregelen (CAPA’s).

REQUIREMENTS

• HBO / WO work and thinking level.
• Demonstrable knowledge and experience with current applicable laws and regulations for medical devices
• By preference a certified lead auditor ISO13485 and demonstrable knowledge of cleanrooms.
• Being able to carry out the work systematically independently and in a team.
• Strong communication skills in word and writing.
• Excellent command of the Dutch and English language in word and writing.

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.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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