SIRE Life Sciences®

QA Manager

Location: Belgium

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 Brussel Belgium.

Medical Devices. No production

ROLE DESCRIPTION

The QA / RA Manager is responsible for establishing and maintaining the global Quality Management System and identifying the opportunities for improvement.

QA is a larger part than RA.

RESPONSIBILITIES

- Implementing, maintaining and controlling a Quality Management System based on ISO9001 and ISO 13485.
- Leading the investigation of NC handling in various tracking systems and following up on the corrective actions,
- Coordinate (FSCA) Field Safety Corrective Actions
- Identifying training needs and recommendations to achieve or maintain necessary employee competencies
- Ensure that inbound inspection is established, implemented and maintained with all related processes at both locations in The Netherlands and Belgium,
- Monitoring performance by gathering relevant data and producing statistical reports,
- Ensuring activities in the quality plans are carried out
- Support on all related CAPA’s
- CAPA coordinator
- Participating in internal and external audits and follow up on the audit findings
- Responsible for monitoring and maintaining quality and compliance targets
- Preparing and analyzing information for the purpose of Management Review

REQUIREMENTS

- Bachelor’s degree in Quality Assurance or related field experience
- About minimum 2 years hands-on experience in Quality Assurance
- Willing to travel (Office in Hilversum and Brussels)
- MS Office, Enterprise Resources Systems (ERP)
- Knowledge of ISO 13485 / ISO9001 / EU regulatory compliance for medical devices
- Excellent Communication skills
- Excellent language skills in French, Dutch and English


FRENCH IS MANDATORY AND THE MOST IMPORTANT LANGUAGE TO SPEAK IN THIS ROLE!!!!!

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.

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

Czy chcesz otrzymywać oferty pracy na podobne stanowiska?

Utwórz powiadomienie e-mail
Zapisz mnie

Zapisani kandydaci otrzymują informacje jako pierwsi.

Podziel się ze znajomymi