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 talented 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 inspired, invested, cared for, valued, and have a strong sense of belonging.

　　What You Can Expect

　　Responsible for assisting the team with regulatory filings as necessary to market Zimmer Biomet products. This is an entry level position, providing training towards full competency in Regulatory Affairs (RA). This position requires a understanding of medical devices and their use as well as a understanding of the regulatory submissions process in Colombia and Latin America. May perform some or all of the following functions, depending on specific assigned focus.

　　How You'll Create Impact

　　Coordinate and assist in the preparation of technical documentation for use in regulatory submissions for product registrations, renewals and registration changes

　　Assist with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified products

　　May aid in regulatory direction to development project teams as a core team member.

　　Maintains registration databases, product registration records, key performance indicators.

　　Follows Zimmer Biomet RA policies and procedures.

　　Miscellaneous responsibilities as assigned.

　　Gather Technical and Legal documents for Global submissions.

　　What Makes You Stand Out

　　Strong writing, communication, and interpersonal skills

　　Strong attention to detail

　　Strong problem-solving and analytical skills

　　Ability to work with rapid changes; flexible and able to balance competing priorities

　　Ability to learn and apply regulations pertinent to medical devices, biologics, drugs and combination products, specific to the product registration process in Latin America

　　Self-motivated and capable to work in a diverse, fast-paced and dynamic environment

　　Ability to build strong relationships; communicate effectively at all levels

　　Basic computer skills, including Microsoft Office Suite

　　Your Background

　　Bachelor’s degree (or non-US equivalent) required; concentration in life sciences, related field preferred.

　　Intermediate English Proficiency is required

　　Travel Expectations

　　Up to 10%

　　EOE/M/F/Vet/Disability