Hiring: Senior Manager, Post-Market Surveillance Company: VERO Biotech Location: Atlanta, GA Job Posted Time: 2026-09-10 10:36:34 About the job Experience: •8+ years in Quality/Regulatory roles in medical device, pharmaceutical, or combination products •3+ years of leadership experience in complaint handling or Post-Market Surveillance Required Skills: •The position ensures compliance with applicable FDA regulations (21 CFR Parts 4, 803, 820, and 210/211 as applicable) and international standards, while driving consistency, inspection readiness, and risk-based decision-making across both sites. •Complaint Handling System Ownership (Multi-Site) •Own and oversee the end-to-end complaint lifecycle across both manufacturing/operational sites, ensuring consistent execution and harmonization. •Establish and maintain a site ownership model (e.g., product ownership vs. investigation ownership vs. reporting accountability). •Ensure appropriate escalation pathways for cross-site complaints and systemic issues. Qualifications: •Bachelor’s degree in engineering, Life Sciences, or related field (master’s preferred) •Excellent communication and leadership skills with the ability to influence senior stakeholders. •Demonstrated capacity to manage multiple priorities and drive execution in a fast-paced environment. Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!