Emploi
Mes offres
Mes alertes emploi
Se connecter
Trouver un emploi Astuces emploi Fiches entreprises
Chercher

Clinical auditing specialist ii - vendor and information system audits team

Bruxelles
ThermoFisher Scientific
Audit
Publiée le Publiée il y a 21 h
Description de l'offre

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as Quality Assurance Auditor II (Technology Solution Audits Team) and enhance our clinical auditing processes by ensuring regulatory compliance and quality standards. What You'll Do: Conduct and/or lead external supplier GxP information systems audits as requested by senior management, including but not limited to on-site, virtual, questionnaire, or desktop audits of technology solutions used in clinical trials Assess processes related to computerized systems used in clinical trials, including Quality Management Systems (QMS), System Development Life Cycle (SDLC), information security, data integrity, business continuity, disaster recovery, backup and restore, and data center and/or cloud hosting environments. Provide GxP regulatory consultation and support to internal project teams and stakeholders on information systems compliance requirements, including but not limited to 21 CFR Part 11 and applicable EMA guidelines for computerized systems used in clinical trials. Prepare, document, and issue audit reports and observations to departmental and cross-functional stakeholders Contribute to team's Practical Process Improvement (PPI) efforts Required Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous QA experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years'). Required Knowledge, Skills and Abilities: Thorough knowledge of GxP and appropriate regional research regulations and guidelines Demonstrated proficiency and led a range of GxP audits to high standards required by management Working knowledge or familiarity with GAMP 5 R2, computer system validation concepts, 21CFR Part 11 Compliance, and the software development lifecycle (SDLC). Excellent oral and written communication skills Strong problem solving, risk assessment and impact analysis abilities Solid experience in root cause analysis Above average negotiation and conflict management skills Flexible and able to multi-task and prioritize competing demands/work load Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience - and where your contributions truly make a difference. Apply today to help us deliver tomorrow's breakthrough! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Postuler
Créer une alerte
Alerte activée
Sauvegardée
Sauvegarder
Offre similaire
(senior) manager technology audit
Zaventem
KPMG
Audit
Offre similaire
Audit supervisor | leadership & groei
Zaventem
Sander Brussels
Audit
Offre similaire
Finance consultant boekhouding & audits – groei & impact
Zaventem
Trifinance
Audit
Offres similaires
Emploi Gestion à Bruxelles
Emploi Bruxelles
Emploi Bruxelles-Capitale
Accueil > Emploi > Emploi Gestion > Emploi Audit > Emploi Audit à Bruxelles > Clinical Auditing Specialist II - Vendor and Information System Audits Team

Jobijoba

  • Dossiers emploi
  • Avis Entreprise

Trouvez des offres

  • Offres d'emploi par métier
  • Recherche d'emploi par secteur
  • Emplois par sociétés
  • Emploi par localité

Contact / Partenariats

  • Contact
  • Publiez vos offres sur Jobijoba

Mentions légales - Conditions générales d'utilisation - Politique de confidentialité - Gérer mes cookies - Accessibilité : Non conforme

© 2026 Jobijoba - Tous Droits Réservés

Postuler
Créer une alerte
Alerte activée
Sauvegardée
Sauvegarder