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As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognized.<br><strong>What You Can Expect</strong></p><p>Position is responsible for post market surveillance (PMS) assignments, including document ownership of initial PMS plans, revised plans, tracking of Post Market Clinical Follow-up (PMCF) commitments and scheduling of PMS review according to the PMS schedule.</p><p><strong>Work Location: Bangalore</strong><br><strong>Work Mode: Hybrid (3 Days in office)</strong></p><p>How You'll Create Impact</p><ul><li>Document owner for Post Market Surveillance Activities; Initial PMS Plans (PMSP) and Review (PMSR) records; responsible for working with Regulatory Affairs to ensure documentation has been reviewed and aligned with Notified Body (when applicable).</li><li>Ensures Post Market Clinical Follow-up (PMCF) commitments are clearly documented within relative PMSPs, informed within clinical research department, and aligned with Notified Bodies.</li><li>Scheduling and coordination of PMS teams for review of proactive and vigilance activities according to schedule; gathering inputs from cross functional stakeholders and elevating at-risk findings to senior management.</li><li>Track execution of PMS plan according to requirements; report to management on track, delayed and at risk PMS commitments; project management of PMS action items to ensure deadlines met.</li><li>Completes routine audits of PMCF commitments against PMSP to ensure quality and transparency of commitments is maintained.</li></ul><p><strong>What Makes You Stand Out</strong></p><ul><li>Strong communication skills, both written and verbal; experienced intrapersonal skills and the ability to influence cross functional stakeholders and work in a fast-paced environment prone to change. &nbsp;Strong attention to detail and ability to manage multiple projects and meet deadlines.</li><li>Thorough knowledge of Global Medical Device regulations relative to Post Market Surveillance (Medical Device Directive &amp; Revisions, ISO 14155, FDA Section 515 &amp; 522, FDA MDR requirements, etc.) is preferred.</li><li>Proficiency with Microsoft Office suite, and advanced spreadsheet or Microsoft Excel experience preferred.</li><li>Demonstrated senior Level capability through autonomous working, strong critical thinking, end?to?end project ownership, and the ability to execute responsibilities independently with minimal supervision.</li></ul><p><strong>Your Background</strong></p><p><strong>Required Skills</strong></p><ul><li>Thorough knowledge of global medical device regulations related to post-market surveillance (Medical Device Directive and revisions, ISO 14155, FDA Sections 515 and 522, FDA MDR requirements, etc.) is preferred.</li><li>Seniority will be determined by level of autonomy, critical thinking ability, project ownership, and the capacity to work independently.</li><li>Excellent English verbal and written communication skills.</li></ul><p><strong>Desired Skills:</strong></p><ul><li>Direct experience with PSURs and PMS plans is preferred; 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