We are ZimVie, a publicly traded, global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients' smiles, function, and confidence. Our company is founded on a legacy of trusted brands, products, and clinical evidence made possible through an inclusive and collaborative culture that empowers our team members to bring their whole selves - their best selves - to work every day to accomplish our Mission. Together, our dedicated, diverse global team is shaping an exciting future for ZimVie - we hope you'll consider being a part of it!

Job Summary:

This position is responsible for supporting the complaint handling unit by assessing complaints for Medical Device MDR / Vigilance reportability of adverse event(s) to the FDA and other National Competent Authorities in the countries in which ZimVie distributes products. This individual executes based on the adverse event determination process with a focus on the defined steps of this process. This position is responsible for decision-making, reassessment, preparation, and submission of adverse event reports globally, as required. Provides guidance and feedback to other team members pursuant to the defined procedures. Responsible for follow-up with division personnel, site team, and international team members to ensure effectiveness and responsiveness related to the adverse event process. Responsible for the communication of data and escalation of potential high-risk complaints to the applicable to site manager and or process owner.

• Adheres to all corporate and site-specific complaint handling procedures.
• Identifies and investigates solutions to procedure and process-related issues. Revises the procedure or process as needed to increase efficiency and compliance.
• Documents and maintains complaint records in accordance with corporate and site-specific procedures.
• Creates, maintains, and monitors appropriate metrics to measure the key performance indicators of the complaint unit.
• Evaluates and assess product complaints to determine adverse event reportability within the complaint-handling process.
• Accurately prepares, generates, and submits initial, supplemental, and final incident reports (e.g., MDR, MDR, etc.) within the regulatory timeframes.
• Provides direction to internal and external personnel on product experience reporting, complaint handling, and adverse event determination.
• Assists Management in special projects, as required.

• Strong organizational and time management skills.
• Strong written, oral, and presentation communication skills.
• Knowledge of Qualityze or similar electronic Quality Management System (eQMS), Livelink, Microsoft Office applications, Oracle, and the ability to learn other software quickly as required.
• Detail-oriented.
• Ability to consistently meet high standards of input accuracy, produce quality documents, compile data, and perform simple analyses with accuracy.
• Strong decision-making skills and proven ability to balance priorities among the many ongoing tasks and being responsive to critical situations, as this position has a high volume of work, regulatory-mandated time limits, and often changing priorities.

• Action-orientated: Ability to take the initiative to correct problems or make changes for improvement without waiting for direction.
• Proven ability to work in a team setting. Willing to share the load and participate in projects outside of normal job scope. Ability to work closely with others to assure functional commitments is met.
• Proven ability to provide training to Team Members as needed.
• Ability to work with all individuals in a congenial and cooperative manner.

• Typically requires Bachelor of Science degree in biology, health sciences, engineering, or nursing preferred or bachelor's degree in another discipline with equivalent years of relevant experience.
• 2+ years' experience required, preferably in the medical device industry.

• Up to 5%

• Requisition ID: 2889