Development Engineer II - Sustaining

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)

Shift Timing: 11:00 AM - 8:00 PM

How You'll Create Impact

Executes sustaining projects with limited supervisionAuthors and releases ECOs; ensures complianceParticipates in root cause and CAPA executionSupports cost reduction and supplier change initiativesIdentifies incremental product/process improvementsContributes 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 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

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 Engineering2 to 5 years of full-time (including relevant Zimmer BiometB Coop/Intern) engineering experience

Travel Expectations

Up to 5%

EOE/M/F/Vet/Disability