At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a general 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 recognised.
What You Can Expect
The Clinical Post Market Surveillance Specialist is document owner for Post Market Surveillance Activities; will document PMS Plans and, if the case, PMS Reviews (PSURs or PMSRs) records according to the applicable regulations (including MDR (EU)
2017/745); he /she will be responsible for working with Regulatory Affairs to ensure documentation has been reviewed and aligned with Notified Body (when applicable). The Clinical PMS specialist will ensures Post Market Clinical Follow-up (PMCF) commitments are clearly documented within relative PMSPs, informed within clinical research department, and aligned with Notified Bodies. Scheduling and coordination of Clinical 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. Track execution of PMS plans according to requirements; report to his / her manager on track, delayed and at risk PMS commitments; project management of PMS action items to ensure deadlines met. Completes routine audits of PMCF commitments against PMSPs to ensure quality and transparency of commitments is maintained.