Development Sr Engineer I Sustaining
Zimmer Biomet · Bengaluru
- Experience5+ yrs
- SalaryNot disclosed
- Work modehybrid
- Levelsenior
- Posted1 Oct 2026
About Zimmer Biomet
Zimmer Biomet is hiring in Bengaluru in healthcare. This role looks for around 5+ years of experience.
Skills
- Microsoft Office Suite
- medical device design and development
- product lifecycle management
The role
A sustaining engineer at a medical technology company leads product improvements and manages medical device design and development with quality and regulatory compliance. Applies geometric dimensioning and tolerancing and manufacturing processes to verification, product lifecycle maintenance, audits, and commercialization.
Full 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
Independently leads small-to-medium sustaining projects and product improvements; provides input for audits. Leads sustaining projects and ensures product lifecycle maintenance and compliance.
Work Location: Bangalore
Work Mode: Hybrid (3 Days in office)
Shift Timing - 11:00 AM - 8:00 PM
How You'll Create Impact
Leads small-to-medium sustaining projectsOwns design changes from initiation through verificationLeads quality/cost improvements across assigned product linesProvides technical input for quality records, audits, regulatory reviewsMentors junior engineersPartners with cross-functional teams to align priorities
What Makes You Stand Out
Independent execution of sustaining projects and product improvements.Ownership of design changes, verification activities, and lifecycle updates.Strong technical problem-solving and quality/cost improvement skills.Ability to provide input for audits, regulatory reviews, and quality records.Mentorship of junior engineers and team knowledge sharing.Influential cross-functional alignment and priority setting.
Your Background
Bachelor's Degree in Engineering or relevant degree and 5 years of relevant experience5+ years of full-time engineering experience.Demonstrated good written and verbal communication skills including presentation skills requiredKnowledge of ASME GD&T standards with application to product design desiredKnowledge of various manufacturing processes (including subtractive machining, anodization, additive manufacturing, forging, casting, plastic molding) and material science for application in new product development desiredFDA QSR and EU MDR medical device regulatory requirements, and industry/regulatory body recognized technical product standards knowledge desiredStatistics knowledge with application to sample size determination and null hypothesis testing desiredMicrosoft Office Suite software proficiency requiredDemonstrated product design and development execution with a multi-disciplinary project team from user need identification/concept ideation through commercialization desired; medical device particularly orthopedic implant and instrument product design desired
Preferred
Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Biomedical Engineering, Bioengineering, Mechatronics Engineering, Aerospace Engineering or Aeronautical Engineering
Travel Expectations
Up to 5%
EOE/M/F/Vet/Disability