More jobs:
Controls Engineer
Job in
New York, New York County, New York, 10261, USA
Listed on 2026-02-16
Listing for:
KKR Consulting
Full Time
position Listed on 2026-02-16
Job specializations:
-
Engineering
Electrical Engineering, Systems Engineer
Job Description & How to Apply Below
KKR Consulting partners with businesses to solve challenges, streamline processes, and achieve lasting success. We specialize in providing tailored consulting services across Aerospace, Medical Devices, Automotives, Pharmaceuticals, and Biotechnology industries, helping clients drive innovation, enhance operations, and achieve sustainable growth.
Job Title:Controls Engineer
Location:
New York (Onsite)
Job Summary
The Controls Engineer will support the design, development, and maintenance of control systems used in medical device manufacturing and product testing. This role is ideal for an early-career engineer with hands‑on exposure to PLC programming and PCB design, looking to grow within a regulated medical device environment.
Key Responsibilities- Assist in the development and support of PLC-based control systems for medical device equipment
- Support PLC programming, troubleshooting, and testing (Allen‑Bradley, Siemens, or similar)
- Assist with PCB schematic design, layout review, and testing
- Support verification and validation (V&V) activities and documentation
- Follow design control and quality system procedures (FDA, ISO 13485)
- Participate in design reviews, risk assessments, and change control activities
- Support manufacturing, automation, and equipment troubleshooting
- Create and maintain technical documentation (drawings, test protocols, reports)
- Bachelor’s degree in Electrical, Controls, Mechatronics, or Automation Engineering (or related field)
- 1–3 years of experience or strong academic/project experience in controls engineering
- Hands‑on exposure to PLC programming
- Basic experience with PCB schematics or layout tools (Altium)
- Understanding of basic electrical and control system principles
- Willingness to work in a regulated medical device environment
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