PCB Layout Engineer III

Overview

PCB layout engineer will design multi layer PCBA's and implement best-in-class systems for medical devices (such as patient monitoring, telemetry or anesthesia) and be part of a world class, highly energized engineering team. Works on projects involving micro-controller, embedded platform and digital circuit design in the development of products - including system and component level design, proto-typing, simulation and component selection.

Responsibilities

Lead advanced PCB design projects using Cadence Allegro and Altium Designer, from schematic capture to layout and release
Architect and implement high-speed digital interfaces, including PCIe Gen2/Gen3, DDR4/DDR5, USB 3.x, and Gigabit Ethernet
Collaborate with cross-functional teams to develop medical-grade electronics, ensuring compliance with IEC 60601, ISO 13485, and FDA Class II/III standards
Perform signal integrity (SI) and power integrity (PI) simulations to validate high-speed performance and reliability
Drive DFM/DFT/DFX reviews and ensure EMI/EMC compliance for regulated environments
Generate complete fabrication and assembly documentation (Gerber, ODB++, BOM, pick-and-place)
Support board bring-up, validation, and design verification testing (DVT) for medical prototypes
Maintain IPC- compliant libraries and contribute to continuous improvement of design processes
Required Skills- Expert-level proficiency in Cadence Allegro (17.x+) and Altium Designer (24.x+)
Proven experience with PCIe layout, differential pair tuning, and impedance-controlled routing
Strong grasp of SI/PI principles, including eye diagram analysis and return path optimization
Familiarity with medical electronics design constraints, including isolation, leakage, and patient safety
Hands-on with multi-layer board design, HDI, and controlled impedance stack-ups
Experience with simulation tools like Sigrity, HyperLynx, or ADS
Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork
Demonstrate behavior consistent with the company’s Code of Ethics and Conduct
It is the responsibility of every employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem
Duties may be modified or assigned at any time to meet the needs of the business

Qualifications

B.E./B.Tech/M.Tech in Electronics, Electrical, or Biomedical Engineering
IPC CID/CID+ certification preferred - Familiarity with medical device lifecycle, risk management, and regulatory documentation Preferred.
Experience in Class II/III medical device development, including ECG, Speciality parameters, or wearable diagnostics.
Exposure to ISO 14971 risk analysis and IEC 62304 software-hardware integration
Knowledge of PLM systems, ECAD-MCAD collaboration, and traceability workflows.

Soft Skills

Excellent communication, interpersonal and leadership skills
Good documentation skills
Self-initiative and self-managed
Voice out issues and persuasive to resolve issues
Good time management and organizational skills
An ability to work to deadlines

Physical Requirements

Standing: 15%
Bending:
Sitting: 70%
Stooping: Reaching:
Walking: 10%
Lifting: (0 – 25lbs)
Use of computer: 70%
Must be able to complete job responsibilities working with global time zone needs such as attending late night/early morning meetings by phone and/or web to meet global business needs: 5%
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