Alcon
Website:
alcon.com
Job details:
Summary of Position:
The Senior Associate 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:
- Support existing electrical and electronic products through board-level testing, troubleshooting, schematic review, failure investigation, and technical documentation updates. This role “does not” include new products or circuit/schematic design activities.
- Use knowledge of electronic boards, wiring, power supplies, sensors, and electrical interfaces to identify and resolve product issues.
- 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 product 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 electrical and electronic product changes continue to meet quality and regulatory requirements.
- 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.
- Perform engineering assessments for sustaining activities, including equivalent component evaluations, electrical and thermal derating, tolerance analysis, signal integrity, manufacturability and assembly reviews, and EMC/EMI analysis.
Key Requirements/Minimum Qualifications:
Minimum Requirements
- Bachelor’s degree in Electrical and Electronics Engineering (EEE) or Electronics and Communication Engineering (E&C)
- 5+ years of experience in medical device sustaining engineering, product support 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.
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