Job Information
Zimmer Biomet Manufacturing Engineer II in Bangalore, India
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
The manufacturing engineer II is responsible for providing manufacturing engineering services to support efficient manufacturing processes. Engineering services may include cell management, process development, project management, process validation, tool design, and trouble shooting.
Work Location: Bangalore
Work Mode: Hybrid (3 Days in office)
How You'll Create Impact
Maintain and improve controlled technical documents such as prints, procedures, bill of materials and routers.
Support a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc.
Conduct feasibility studies to estimate product cost and analyze capital equipment, capacity, and capability requirements.
Improve process methods which meet performance and quality requirements.
Execute to project plans and schedules for work activities.
Communicate (written and verbal) with appropriate personnel from other departments.
Partner with cross-functional departments to make process and procedure recommendations.
Provide training and guidance to entry-level engineers.
This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.
What Makes You Stand Out
Skilled and knowledgeable in manufacturing and new product processing
Competence with drafting standards and geometric dimensioning and tolerancing
Ability to balance marketing, manufacturing, and design requirements to meet customer requirements
Ability to lead and prioritize multiple medium complexity project assignments and complete work in a timely manner
Good problem-solving skills through the use of quality and statistical tools
Ability to effectively work within a cross-functional team to complete critical project tasks
Demonstrates good written and verbal communication skills
Experienced with control procedures, such as the Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions.
Proficient with Statistical Process Control concepts, process development, CNC programming terminology, and tooling design concepts
Microsoft Office Suite and Project
Your Background
Required Technical Skills
Experience in Manufacturing Engineering within a medical device or regulated manufacturing environment
Strong understanding of design requirements and ability to translate them into manufacturing and risk documentation (DHF / RMF), Strong exposure to ECR(Engineering Change Request), ECO(Engineering Change Order), ECN(Engineering Change Notice)with impact analysis and cross-functional approvals.
Hands-on experience with change control processes and documentation updates
Working knowledge of PLM systems (Windchill preferred) , teamcenter or any other tool.
Ability to collaborate with cross-functional teams, manage intake requests end to end, and provide clear status updates
Education and Experience Requirements
- B.S. in Engineering with a minimum of 1-year experience in an engineering role.
Physical Requirements
EOE/M/F/Vet/Disability