Quality | Post Market Complaint Data Analyst | Orthopedics

Post Market Complaint Data Analyst | Orthopedics

Hybrid (Florida) or US Remote | $80k - 120k base + bonus + benefits

Complaint handlers find the problems. Engineers fix them. You prove whether the fix worked.

Our client is an orthopedic device manufacturer is building out its post-market team, and this analyst seat sits at the center of it. You’ll report to the Senior Director and work every day with complaint handlers and investigation engineers. Your data will drive root cause, CAPA and regulatory decisions, not just fill a database.

What you’ll own

• Complaint data from intake to insight: collecting, cleaning, analyzing and keeping it audit-ready
• The tracking and trending the team runs on, including Excel pivots, charts and dashboards
• Data for international vigilance submissions, mainly EU MIRs under EU MDR
• Your seat at trending reviews, root cause investigations and CAPA discussions
• Clear, defensible reports for Quality, Regulatory, R&D and external stakeholders

What you’ll bring

• 2+ years of data analysis in medical device, pharma or biotech
• 2+ years in post-market complaint handling, investigation or analysis
• Strong Excel skills. SAS, R or Python are a bonus
• Working knowledge of FDA 21 CFR 820/803 and ISO 13485. EU MDR vigilance exposure sets you apart
• A BS in Biomedical Engineering, Life Sciences, Data Science or similar, or equivalent experience

Why this one

A growing team where your work is visible to senior leadership, real exposure to global vigilance, and a clear path into broader post-market quality roles.

Interested, or know someone who’d be a fit? Apply here or message me for a confidential conversation.