Senior Consultant - MedTech QMS Complaints at Veeva

You're a seasoned consultant with over 8 years in GMP systems or software consulting and at least 5 years focused on Medical Device Complaints Management. **What makes it worth a look...** Veeva, a pioneer in industry cloud for life sciences, is offering a fully remote Senior Consultant role in Minneapolis, with a base salary range of $80,000 to $200,000 per year. They are a public benefit corporation committed to balancing stakeholder interests and have a "Work Anywhere" policy. **You might be a good fit if you...** * Have 5+ years of experience in Complaints Management for Medical Device. * Possess a strong understanding of FDA and EU MDR/IVDR reporting requirements. * Are knowledgeable about ISO 13485, 14971, and relevant FDA regulations (21CFR Part 803, 820, 822, 806). * Understand the relationship between Complaint Handling, CAPA, Nonconformance, and Risk Management.