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

- Solid 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.

📌 Systems Engineer & Lead Systems Engineer (Hyderabad)
🏢 Renechip
📍 Hyderabad