Role Overview
We’re looking for a Senior Manager to lead a global team that turns post-market data into timely, reliable and actionable intelligence. This is a high-impact leadership role at the intersection of post-market surveillance, complaint analytics, digital enablement and process transformation.
What You Will Do
You’ll lead the global operating model for post-market monitoring, trending, signal detection and escalation, translate complaint data into clear insights, oversee post-market surveillance plans and reports, and act as business leader for post-market tools and digital capabilities.
Why It Might Be a Fit
You’ll have a minimum of 10 years’ experience in Quality, Post-Market Surveillance, Complaint Management, Vigilance, Regulatory Affairs or a related function, and at least 5 years’ people leadership experience.
Requirements
- A minimum of 10 years’ experience in Quality, Post-Market Surveillance, Complaint Management, Vigilance, Regulatory Affairs or a related function within the medical device or pharmaceutical industry
- At least 5 years’ people leadership experience, with evidence of coaching, developing and guiding teams through change
- Strong hands-on knowledge of post-market surveillance, complaint analytics, product monitoring, trending, signal detection and escalation processes
- Working knowledge of ISO 13485 requirements, particularly complaint handling, data analysis, CAPA, risk management and post-market activities
- Working knowledge of EU MDR requirements relating to post-market surveillance, PMCF, PSURs, vigilance, trend reporting and post-market data evaluation
- Understanding of statistical and risk-based approaches used for complaint trending, signal detection and product monitoring
- Experience implementing analytics, dashboards, reporting, digital or AI-enabled solutions within a regulated environment
- Experience leading process improvement, remediation, compliance transformation or global cross-functional initiatives
- Experience supporting regulatory inspections, notified body assessments, customer audits or agency interactions
- Bachelor’s degree in Engineering, Life Sciences, Statistics, Data Analytics, Quality, Regulatory Affairs, Business or a related STEM field
- A master’s degree, MBA or equivalent advanced qualification would be advantageous
- Professional certifications such as ASQ CQE/CQM, RAC, PMP, Lean Six Sigma Green Belt or Black Belt, or an equivalent qualification, would be beneficial
Benefits
- Dental insurance
- Vision insurance
- Flexible working hours
- Remote work
- Occasional onsite presence
- Travel opportunities
- Competitive salary
- Benefits package
To apply for this job please visit convatec.wd1.myworkdayjobs.com.

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