Quality Business Partner - Medtech
Uniphar
Dublin
Full-time
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Responsibilities
- Act as a Quality subject matter expert (SME) across all MedTech teams.
- Act as a point of contact for all quality matters across EU Medtech business.
- Work closely with business and/or Third\-Party teams to provide expert quality information and support continuous improvement.
- Provide proactive Quality input into new business models.
- Evaluates, and/or reviews procedures and other activities in support of an integrated, cross functional QMS.
- Fosters a commitment to quality in individuals and a culture of quality across the MedTech business.
- Facilitates effective communication and knowledge sharing across teams to promote a culture of quality.
- Ensures rapid communication of quality issues and risks to appropriate management and leaders.
- Ensures rapid communication of quality issues and risks including potential misconduct to appropriate leaders and colleagues.
- Support with the management of intercompany agreements and quality agreements.
- Support with deviation investigations and CAPAs.
- Support with the raising of change controls and risk assessments.
- Ensure distribution and product compliance.
- Provide guidance on MDR and supplier oversight.
- Support audit readiness.
- Partner with cross\-functional teams.
- Drive continuous improvement initiatives.
- Promote a proactive quality culture.
- Support development of quality KPIs and reporting.
- Quality Questionnaire / tender support
- Minimum 3 years’ experience in Medical Devices, MedTech or Pharma distribution
- Strong working knowledge of ISO 13485, MDR requirements, and distribution regulations (e.g., WDA)
- Experience in QMS processes, audits, CAPA, deviations, and supplier management.
- Excellent communication, influencing and stakeholder‑engagement skills.
- Strong analytical, problem‑solving, and organisational abilities.
- Clean drivers licence and ability to travel. Travel across sites in both the domestic and European regions may be required.
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