Biomedical Engineer Lead — Product & Design

Baxter International Inc.; Deerfield (IL); On-site; USD 112,000 - 154,000; Full time

Benefits offered by this job

Medical and dental coverage from day 1

ESPP (employee stock purchase plan)

401(k) with company match

Paid time off 20–35 days

Flexible Spending Accounts

Parental leave

Commuting benefits

Job summary

Baxter International Inc. is seeking a senior design engineer for the Advanced Surgery business. You will apply design controls, CAPA, and cross-functional collaboration to drive development and sustaining engineering.

You will lead technical oversight, review design changes, and ensure FDA/ISO design control compliance while crafting DHF documentation and study plans. A strong background in biomedical/mechanical engineering and CAD is required.

Qualifications

• B.S. in engineering with 5+ years in product development, or MS/PhD with 3+ years.
• Experience creating/managing design documentation and transfer to manufacturing.
• Proficient in 3D CAD software and prototyping/testing of mechanical designs.
• Strong written and verbal presentations within business/technical communities.
• Self-motivated, resourceful, and flexible; able to work independently.

Responsibilities

• Achieve technical outcomes through Design Control, CAPA, CC deliverables within time and budget.
• Provide technical oversight of a changing R&D portfolio impacting multiple functions.
• Lead cross-functional collaboration to meet schedules and project demands.
• Review and approve design changes; provide technical direction to project teams.

Skills

Design Control

CAPA

Cross-functional

3D CAD

Prototyping

Technical oversight

Documentation

Education

B.S. in Engineering

MS/PhD in Engineering

Tools

CAD Software

Job description

Baxter International Inc. is seeking a senior design engineer for the Advanced Surgery business. You will apply design controls, CAPA, and cross-functional collaboration to drive development and sustaining engineering.

You will lead technical oversight, review design changes, and ensure FDA/ISO design control compliance while crafting DHF documentation and study plans. A strong background in biomedical/mechanical engineering and CAD is required.