Growth-Driven QA Specialist - Life Sciences (Hybrid)

EPM Scientific

Tessenderlo

Hybride

EUR 59 000 - 72 000

Plein temps

Il y a 9 jours
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

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Avantages offerts par ce poste

Hybrid work arrangement
Career progression opportunities

Résumé du poste

EPM Scientific in Tessenderlo, Belgium, is seeking a Quality Assurance professional to maintain and improve the site's quality systems, ensuring regulatory compliance and driving continuous improvement.

You will coordinate CAPAs, audits, non-conformities, and document control across functions, with hybrid on-site two days per week, and a clear progression path in a growing life sciences company.

Qualifications

  • Quality Assurance experience within Medical Devices or a regulated life sciences environment.
  • Knowledge of Quality Management Systems (QMS).
  • Experience managing CAPAs, non-conformities, investigations, and document control activities.
  • Experience supporting audits and compliance activities.
  • Fluent English required; additional European languages are advantageous.

Responsabilités

  • Manage quality documentation and document control processes.
  • Support the maintenance and continuous improvement of the Quality Management System (QMS).
  • Lead and coordinate CAPA activities and follow-up actions.
  • Support internal and external audits.
  • Investigate and manage non-conformities and quality events.
  • Ensure compliance with quality standards, regulatory requirements, and internal procedures.
  • Collaborate with cross-functional teams to drive quality improvements.
  • Support quality and compliance initiatives across the organisation.

Connaissances

Quality Assurance
QMS knowledge
CAPA management
Audits support
Documentation control

Description du poste

EPM Scientific in Tessenderlo, Belgium, is seeking a Quality Assurance professional to maintain and improve the site's quality systems, ensuring regulatory compliance and driving continuous improvement.

You will coordinate CAPAs, audits, non-conformities, and document control across functions, with hybrid on-site two days per week, and a clear progression path in a growing life sciences company.

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