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
Executes sustaining engineering projects with limited supervision; authors and releases Engineering Change Orders (ECO)s ensuring compliance. Supports sustaining projects and executes design updates to maintain compliance and product performance.
Work Location: Bangalore
Work Mode: Hybrid (3 Days in office)
How You'll Create Impact
- Executes sustaining projects with limited supervision
- Authors and releases ECOs; ensures compliance
- Participates in root cause and CAPA execution
- Supports cost reduction and supplier change initiatives
- Identifies incremental product/process improvements
- Contributes to standardization of sustaining documentation
What Makes You Stand Out
- Solid engineering analysis and problem-solving to support sustaining tasks.
- Competent in drafting, authoring, and releasing compliant ECOs.
- Ability to participate in CAPA/root-cause investigations.
- Familiarity with cost-reduction, supplier changes, and process improvements.
- Effective communication with cross-functional partners.
- Ability to organize documentation and standardize sustaining practices.
Your Background
- Demonstrated good written and verbal communication skills including presentation skills required
- Knowledge of ASME GD&T standards with application to product design desired
- Knowledge of various manufacturing processes (including subtractive machining, anodization, additive manufacturing, forging, casting, plastic molding) and material science for application in new product development desired
- FDA QSR and EU MDR medical device regulatory requirements, and industry/regulatory body recognized technical product standards knowledge desired
- Statistics knowledge with application to sample size determination and null hypothesis testing desired
- Microsoft Office Suite software proficiency required
- Demonstrated 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
Qualifications
- Bachelor's Degree in Engineering or relevant degree and 1 year of relevant experience
Preferred
- Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Mechatronics Engineering, Aerospace Engineering or Aeronautical Engineering
- 1 to 3 years of full-time (including relevant Zimmer BiometB Coop/Intern) engineering experience
Physical Requirements
Travel Expectations
Up to 5%
EOE/M/F/Vet/Disability
