What You Can Expect

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.
• Assist in the review and evaluation of promotion and advertising material for compliance with applicable regulations
• Follows Zimmer Biomet RA policies and procedures.
• Gather Technical and Legal documents for Global submissions.
• Miscellaneous responsibilities as assigned

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, or related field preferred.
• 3 Years of Experience
• Advanced English Proficiency is required

Travel Expectations