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

 

Supports the identification and development of new technologies related to biosensors, infection management, biomaterials and tissue repair.Serves as a subject matter expert, contributing to and collaborating on new product development projects involving biocompatibility, chemical analysis, and mechanical testing. Acts as a scientific advisor to functions such as Development, Manufacturing, Quality Assurance, Regulatory, Marketing, Sales, Clinical Affairs, and Business Development (not exhaustive).Maintains close collaboration with other Zimmer Biomet sites and external suppliers. Supports Master's and PhD research projects at partner universities, actively seeking opportunities for academic collaboration and external funding.Delivers training for both Team Members and Customers.How You'll Create Impact

 

Support the identification and development of technologies in areas such as infection management, biomaterials, tissue repair and regeneration, and emerging non-material-based innovations (e.g. biosensors).Conduct technology scouting by monitoring trade publications, academic journals, and university research activity, and disseminate relevant findings within the organisation.Contribute to New Product Development (NPD) by supporting biocompatibility assessments, mechanical testing, and risk management activities.Support regulatory submissions to Notified Bodies and other global regulatory authorities.Author technical protocols, scientific reviews, product specifications, and other documentation required for regulatory submissions.Support Manufacturing by investigating and resolving technical issues, exploring new manufacturing methods, and validating processes and equipment through testing.Provide Sales and Marketing support through employee and surgeon training, development of technical marketing materials, and by delivering presentations at Zimmer Biomet meetings as part of the faculty.Deliver cross-functional training for internal and external personnel in Manufacturing, QA, Regulatory, NPD, Marketing, and Sales.Support Business Development by addressing technical queries during due diligence activities.Oversee external laboratory testing and analysis.Review and update internal procedures to ensure alignment with evolving ISO and ASTM standards.Represent Zimmer Biomet at scientific societies and international meetings through presentations and technical contributions.Maintain up-to-date scientific and medical knowledge by attending relevant conferences, courses, and meetings.Provide technical support for external collaborators through meetings and site visits.Explore opportunities for academic collaboration with universities and research laboratories.Identify opportunities for external research funding.Support university-based research projects at Master’s and PhD levelWhat Makes You Stand Out

 

Serves as a key contributor to research and product development projects, providing technical leadership and subject matter expertise.Experienced in collaborating with universities and external laboratories on research activities and innovation programmes.Acts as a specialist and internal consultant, with the ability to navigate and engage both internal and external networks to obtain critical information and insights.Solves complex challenges related to analytical testing, manufacturing processes, and quality assurance.Demonstrates strong written and verbal communication skills, including the ability to deliver clear, confident, and audience-appropriate scientific presentations.Possesses in-depth knowledge of testing methodologies, materials research, and cross-functional processes.Capable of designing robust testing plans and experiments, with sound judgement on which evaluations are critical for project progression.Maintains a solid working knowledge of relevant industry standards (e.g. ISO, ASTM) and applies them effectively in day-to-day work.Strong analytical and problem-solving capabilities; able to evaluate multiple dimensions of a problem and implement timely, practical solutions.Proactively advances methods and knowledge within the team - establishing new approaches and frameworks for future work (\"trailblazing\").Takes ownership of the quality and integrity of personal work and contributes to maintaining high standards across project teams.Familiar with intellectual property (IP) databases and the principles of IP protection and management.Works independently, demonstrating foresight and the ability to anticipate and mitigate potential issues.Continuously seeks and identifies opportunities to improve departmental practices and outcomes.Balances the needs of multiple departments to meet project timelines and customer expectations.Plans and utilises resources effectively, ensuring efficient and timely execution of project tasks.Communicates professionally, concisely, and with sensitivity when engaging with colleagues and stakeholders.Handles complex technical discussions with confidence and clarity.Demonstrates strong initiative and a proactive approach to problem-solving and innovation.Your Background

 

A higher degree (Master’s or PhD) in a relevant scientific or engineering discipline, such as Bioengineering, Biomaterials, Materials Science, or Mechanical Engineering. A higher degree project related to biosensors is preferred.Demonstrated leadership or significant contribution to complex, high-impact projects within the medical device industry or academic research environments.A strong record of internal and external training relevant to their area of expertise.Proven ability to present technical data clearly and persuasively to expert audiencesSkilled in communicating complex scientific concepts in an accessible and engaging manner, with experience presenting at research meetings and scientific forums.

EOE/M/F/Vet/Disability