Senior Electrical and Electronics Engineer

Sr. Associate I, Research & Development Process & Product Design

Summary of Position:

The Senior Engineer I – Electrical & Electronics (E&E) is responsible for sustaining engineering support for electrical and electronic systems for ophthalmic medical devices. This role ensures product continuity, compliance, and performance throughout the product lifecycle and acts as a technical interface with cross functional stakeholders including Software Lifecycle Management (LCM), Design Control, Manufacturing, Service, Quality, Regulatory Affairs, Medical Safety and Clinical teams.

Key Responsibilities:

• Provide subject matter expertise for electrical and electronic systems, including PCBAs, electrical assemblies, wiring, power systems, sensors, and interfaces
• Review and assess engineering changes (ECOs/ECNs) impacting E&E scope, including risk, compliance, verification, and implementation readiness
• Support design control activities related to E&E, including requirements, risk analysis, verification, and traceability
• Perform root cause analysis and technical investigations for field, manufacturing, and service‑related electrical issues
• Evaluate component changes, obsolescence, and supplier impacts and recommend technically sound solutions
• Assess material compliance impacts (e.g., RoHS, REACH, and region‑specific regulations) associated with component and supplier changes
• Ensure continued regulatory and quality compliance throughout the product lifecycle
• Collaborate effectively across mechanical, software, systems, manufacturing, quality, and regulatory teams to resolve complex issues
• Provide engineering judgment and recommendations, proposing alternative solutions when required
• Support Technical file reviews and updates, ensuring alignment with county specific regulatory requirement (e.g., US, EU, China), in collaboration with Regulatory Affairs.
• Support product complaint investigations and assess the need for updates to Risk Management Report (RMR), in collaboration with Complaints, Medical Safety and Design Control teams.

Key Requirements/Minimum Qualifications:

Minimum Requirements

• Bachelor’s degree in Electrical / Electronics Engineering or a related discipline
• 5+ years of experience in medical device sustaining engineering or product development

Preferred Experience

• Experience supporting embedded electronic systems
• Proficiency with PLM and requirements tools (e.g., Windchill, Polarion, Teamcenter)
• Working knowledge of systems engineering principles and interface management
• Exposure to surgical or ophthalmic medical devices
• Familiarity with medical device standards such as ISO 13485, ISO 14971, and awareness of electrical safety and EMC requirements (e.g., IEC 60601 series).

KNOWLEDGE, SKILLS & BEHAVIORS

• Strong analytical and structured problem-solving skills
• Ability to work independently with moderate autonomy while following defined processes
• Effective communicators in cross functional and global environments
• Collaborative team player with ownership mindset
• Product lifecycle and business awareness
• Quality driven, compliance focused approach

Work hours: 1 PM to 10 PM IST

Relocation assistance: Yes

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Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.

Experience Level

Mid Level