Senior Manager Quality Assurance
Panda International
Senior Manager Quality Assurance
Samenvatting
Wat krijg je?
Wat ga je doen?
- Regionale kwaliteit- en compliancestrategie bepalen
- Toezien op het volledige QMS-beheer
- Leverancierskwaliteit en productcompliance waarborgen
- Design controls en risicomanagement beheren
- Samenwerken met diverse interne belanghebbenden
Wat verwachten wij?
- 10 years experience in medical device quality
- Expertise in EU MDR and ISO 13485
- Leadership experience across multiple teams and locations
- Experience with DHF and design controls
Volledige vacaturetekst
As the Senior Manager of Quality Compliance EMEA, you will spearhead the quality strategy and QMS performance for a leading international medical device organisation. This high-impact leadership role offers full ownership over regional compliance and supplier quality within a globally connected business where innovation thrives. You get the unique chance to shape strategy and drive transformation across multiple sites. Discover how your expertise can make a lasting impact.
Senior Manager of Quality Compliance, EMEA (Medical Devices)
I’m currently partnering with a leading international Medical Device organisation to appoint a Senior Manager of Quality Compliance, EMEA. A senior leadership role with full ownership of quality strategy, compliance, and QMS performance across the region.
This is a high-impact position where you’ll lead QMS, Supplier Quality, and Divisional QA teams, ensuring compliance with EU MDR 2017/745, ISO 13485, and global standards, while driving continuous improvement and operational excellence across multiple sites.
Key focus areas:
• Leadership of regional Quality & Compliance strategy across EMEA
• Oversight of QMS (CAPA, audits, change control, management review)
• Supplier quality and finished goods compliance
• Design controls, risk management (ISO 14971), and product lifecycle quality
• Cross-functional collaboration with RA, R&D, Operations, and global stakeholders
• Leading audits (Notified Bodies, authorities, customers) and regulatory readiness
• Driving harmonisation and simplification of QMS across sites
What we’re looking for:
• 10+ years in Medical Device Quality (Class I/II preferred)
• Strong expertise in EU MDR, ISO 13485, and end-to-end QMS
• Proven leadership experience across multiple teams and locations
• Track record in building quality culture and influencing senior stakeholders
• Strategic mindset with hands-on execution capability
• Expertise with product development activities, including DHF, design controls..
Why consider this role?
You’ll be joining a growing, globally connected business where quality is at the core of innovation and market expansion, offering real scope to shape strategy, lead transformation, and make a lasting impact.
If this sounds like you (or someone in your network) feel free to reach out for a confidential discussion.
#MedicalDevices #QualityLeadership #QMS #RegulatoryAffairs #Hiring #EMEA
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