Manufacturing Engineer I
Zimmer Biomet — Bengaluru, Karnataka
₹3–7 LPA (HireSetu estimate) · Entry level · Freshers eligible · Full-time · hybrid
HireSetu listing reference 9a9b3d — confirm requirements below, then apply on the employer site.
Quick answer: A hybrid Bengaluru role where the daily work is BOMs, routers, prints and part numbers for a medical device manufacturer. The background section asks for Windchill, JDE and past Zimmer Biomet project work, so a fresher has to show those somewhere.
From Zimmer Biomet's job posting
Career Opportunities: Manufacturing Engineer (10616)
Requisition ID 10616 - Posted 10/22/2026
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 I is responsible for supporting manufacturing engineering to ensure 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)
Shift Timing - 3:00 PM - 12:00 AM
How You'll Create Impact
Assist in maintaining and improving controlled technical documents such as Tooling/Fixture prints, procedures, manufacturing aids, bill of materials and routers, utilizing Windchill JDE, Vault and Teamcenter.
Support a wide variety of processing applications such as machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, materials, etc.
Item Number Assigment of new part numbers.
Creation/Update Material Description Cards (MDC’s), Manufacturing Material Impact Assessment (MMIA), and Measurement Instruction Sheets (MIS)
Collaborate with Manufacturing, Quality, Regulatory, and Engineering teams to ensure timely closure of changes and documentation accuracy.
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.
Maintain and improve controlled technical documents such as prints, procedures, bill of materials and routers.
What Makes You Stand Out
Ability to balance quality, compliance and safety to meet customer requirements.
Ability to handle 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 teams to complete critical project tasks.
Demonstrates good written and verbal communication skills.
Microsoft Office Suiteand Adobe Acrobat.
Knowledge of Zimmer Biomet Systems..
Your Background
B.S. in Engineering required.
Travel Expectations
Up to 10%
The employer’s company overview, benefits, equal-opportunity statement and generic skills tables are left out here; they are on the original posting.
Text from Zimmer Biomet's official job posting, formatted by HireSetu. The employer's own page is the final word on details.
Paperwork the floor and the auditors both read
The duties lean heavily on controlled documents: bill of materials, routers, tooling and fixture prints, procedures, and new item numbers for parts. Then MDCs, MMIAs and measurement instruction sheets, which record what a part is made of and how it gets measured. At a medical device company those records are what an auditor opens first, so a stale revision or a wrong BOM line is a compliance problem, not a typo. Expect change requests that need Quality and Regulatory sign-off, and a fair amount of chasing people to close them.
Windchill and JDE come first
The background section names Windchill and JDE as required, with Vault or Teamcenter as good to have. It also asks for experience in Zimmer Biomet projects, which reads like it was written with contractors and internal people in mind. As a fresh graduate, state which of those systems you have actually opened, even in an internship or a college project, and what you did in it. Windchill and Teamcenter are PLM tools; JDE is ERP. Knowing how a BOM is structured and what an engineering change order contains costs you an evening and makes the rest of the listing readable.
A late shift, two days from home
The hours run 3:00 PM to 12:00 AM, which puts this team in step with a US working day from Bangalore. Three days in office leaves two late nights worked from home. Check how transport works for a midnight finish before you accept, because that single detail decides whether the schedule holds up over months. Travel is listed at up to 10%.
The title covers more than the production line
Cell management, tool design, process validation and troubleshooting all appear, so there is genuine shop-floor work in the mix. The listed duties still sit mostly in documentation and change control for a global manufacturing group. Someone picturing cycle-time studies and line trials all day will find a quieter, more administrative week here, and the process development and validation exposure is the part that carries you toward a plant-side role later.
Prepared from Zimmer Biomet's job posting and checked against it before publishing. See our Editorial Policy.
How to apply
- The Apply button opens this job on Zimmer Biomet's careers site (career8.successfactors.com).
- Its requisition number is 10616; search for it on the careers site if the link ever stops working.
- You need a candidate account on this careers site before the form opens.
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