Quality Systems Manager
SIRE
Wavre, Belgium
2 dagen geleden

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 organisation, based in Waals-Brabant Belgium.

Role Description

The Quality Systems Manager will be part of the Quality Assurance Department and will report into the Head of Quality. Under the direction of the reporting manager, he / she will continuously improve Compliance systems, strengthen quality awareness and investigate quality issues using applicable process improvement and problem solving techniques to assure successful outcomes of Company and external Health Authority inspections

Responsibilities

Actively contribute to continuous improvement

oDeveloping and implementing a Quality System based on Business process approach

oManaging Operational Excellence initiatives

  • Manage the requalification plan to maintain the accurate validation / qualification state of facilities and systems.
  • Collaboration and participation in projects as Quality Representative for equipment / systems validation / qualification.
  • Provide quality guidance for the development of the validation approach.
  • Assure requirements traceability throughout the whole project validation file
  • Ensure the review / approval of documentation pertinent to equipment / systems validation / qualification is timely performed to achieve compliance to procedures and regulatory requirements
  • oEngineering degree

    o8 years experiences with 3 years in an operational role in a GMP environment

    oVery good knowledge of GxP in a regulated environment

    oKnowledge of risk assessment / validation / quality systems

    oExcellent accuracy and attention to detail

    oExcellent interpersonal skills

    oStrong problems solving skills, issue resolution and root cause analysis

    oHighly Flexible and Adaptable. Able to work independently in a fast paced multitasking environment

    oWorking knowledge of computer packages

    oKnowledge of Quality Software Systems( Trackwise , Lab software , ) is an asset

    oLanguage : English , French

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

    Solliciteren
    Bij de favorieten invoegen
    Verwijder van favorieten
    Solliciteren
    Mijn E-mail
    Door op "voortzetten" te klikken, gaat u ermee akkoord dat neuvoo uw persoonlijke gegevens verzamelt en verwerkt die u in dit formulier hebt verstrekt, om een ​​neuvoo-account te maken en u te abonneren op onze e-mailwaarschuwingen, in overeenstemming met ons Privacybeleid . U kunt uw toestemming te allen tijde intrekken door te volgen deze stappen .
    voortzetten
    Aanvraagformulier