Systems Engineer & Lead Systems Engineer

Face-to-face interview date: Sunday, 20 September 2026, in Hyderabad. Please apply only if you are available to attend the in-person interview on this date; others are requested not to apply.
Location: Hyderabad
Employment Type: Full-Time
Work Mode: Work from Office
Experience: 4–14 Years
Notice Period: Immediate to 15 Days
Interview Date and time: Face to face,@20.09.2026,Hyderabad
## Job Summary
We are looking for an experienced *Systems Engineer / Lead Systems Engineer* with strong expertise in product requirements, requirements traceability, verification documentation, risk management, and medical device design controls.
Key Responsibilities
* Review, analyze, and update product requirements to ensure completeness, consistency, and compliance with applicable quality and medical device standards.
* Perform requirements remediation and establish end-to-end traceability between user needs, system requirements, design inputs, risk controls, verification activities, and evidence.
* Manage requirements, traceability links, test records, risk artifacts, and engineering documentation using *Codebeamer ALM*.
* Review and align verification documentation, test evidence, and verification records with design control requirements.
* Support risk management activities, including FMEA, hazard analysis, risk-control linkages, and risk traceability matrices.
* Collaborate with SMEs, Quality Engineering, Regulatory Affairs, Product Development, Verification, and Systems Engineering teams.
* Support defect review, issue resolution, and documentation updates related to requirements remediation.
* Participate in design reviews and document review sessions to ensure consistency across requirements, verification, and risk management documentation.
* Perform impact assessments and support engineering change documentation when required.
Required Skills
* Strong experience in *Systems Engineering and Requirements Management*.
* Hands-on experience with *Codebeamer ALM* for requirements and traceability management.
* Good knowledge of requirements remediation and end-to-end traceability.
* Experience with verification documentation, test evidence, and design control processes.
* Knowledge of *FMEA, hazard analysis, risk management, and risk-control traceability*.
* Understanding of medical device standards and quality system requirements.
* Strong documentation, analytical, and cross-functional collaboration skills.
Qualification
*B.E./B.Tech or Master’s Degree* in Systems Engineering, Electronics, Electrical, Mechanical, Biomedical Engineering, or a related engineering discipline.

Work arrangement
No