Job Description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. 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 recognised.

What You Can Expect

Primarily responsible for ensuring that Zimmer Biomet records are updated and maintained robustly through the change control process.

How You'll Create Impact

• Executes day to day needs of the department through responding to change control documents requiring document control input, responding to requests from the business and ensuring changes are of high quality.
• Formats and edits Zimmer Biomet work instructions which are being updated in order to ensure company documentation is accurate and consistent.
• Updates Livelink, the Vault and other Zimmer Biomet software systems with newly revised or created documents such as work instructions
• Updates department documentation by routing change requests to create, revise or obsolete documentation control specific work instructions
• Completes scanning of some documentation to ensure that paper based records are maintained

This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA.

What Makes You Stand Out

• Ability to objectively deal with individuals using appropriate tact and diplomacy to establish and maintain a congenial relationship.
• Good verbal and written communication skills.
• Good word processing and database skills.
• Outstanding organizational skills and high attention to detail.
• Knowledge of current Food and Drug Administration (FDA) laws, regulations and practices a plus.

Your Background

• High School education or equivalent plus three years previous regulatory/quality or related experience and or an equivalent combination of education and experience.

Travel Expectations

• Up to 5%

EOE/M/F/Vet/Disability