Specialist in Quality Systems

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 and Pharmaceutical organization, based in Belgium.

Part of a multinational, this division is focused on the distribution of medical devices. The organisation has been active within this industry over many years and became one of the biggest players worldwide. Next to medical devices they are also specialized in pharmaceutical and consumer products. Apply now to become part of this organisation and bring your career to the next level.

ROLE DESCRIPTION

You will become part of a dynamic and technology- driven business setting. As a specialist, you are guiding and directing a team of professionals that focuses on quality and compliance at the distribution site. Together, your aim is to improve quality systems in which you are supported by internal and external stakeholders. You play a major role when it comes down to serving the customers of this organisation. You are a point of contact when it comes down to the distribution site. You will be in charge of tracking and tracing the latest changes within quality and legislation on an international scale. This project lasts for 9 months, with a possibility for extension.

RESPONSIBILITIES

As a quality system specialist, you are responsible for the Quality Management Systems in general. You will receive the responsibility to maintain, asses and improve the QMS, and keep on track of relevant changes and specifications applicable to the system. Furthermore, your role includes:
• To be aware of the internal and external regulations including ISO qualifications.
• To overview processes and applications conducted by your team which includes Audits, CAPA, Document control, risk- and supplier management.
• Constantly analyzing the data and processes to trace risks and identify improvements.
• Maintenance of relationships with both internal and external stakeholder
• Keeping on track with the KPI’s of the quality department
• Development and execution of training directed across departments
• Main contact person for notified bodies and other authorities

REQUIREMENTS

• Master of Science
• Minimal 3 years of experience in the Medical Devices industry
• Minimal 3 years of experience in Quality Assurance within the Life Sciences industry
• Excellent analytical and problem-solving skills
• Fluency in English, French and Dutch
• Minimal 2 years of experience in a leadership role
• Strong in communication and establishment of relationships with various stakeholders

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.