Associate I

The role provides day-to-day case monitoring, assessment and reporting of quality and adverse event complaint records involving Alcon manufactured products and responds to complaint activities required to comply with local and international regulations, guidelines, and applicable directives. This role may be required to work in shifts.
- Process case files according to Standard Operating Procedures (SOP).
Work with affiliate offices to ensure required dataset has been received/requested.
Re-assess the data, ensure accurate product selection and assign required event code(s) in the system.
Complete initial and follow-up reporting assessments as information is received (initial report, follow-up questionnaires, phone calls, investigation findings).
Respond to Manufacturing Quality Assurance (QA) requests and Health Authority inquiries
Launch required quality investigation records.
Schedule expedited and periodic regulatory reports based on local and international reporting regulations.
Perform and receive quality feedback on case management and coding.
Adherence to all corporate compliance guidelines & corporate programs .
Maintains a working knowledge of the following:




Alcon Products for assigned therapeutic areas and corresponding documentation (Product Information, Directions for Use, Manuals, Promotional materials)
Eye anatomy
Common diseases
Ophthalmic evaluation procedures
Eye terminology and abbreviations
Safety database(s) and reporting tools
Process and review Surgical – Intra Ocular Lens (IOL) complaint records in accordance with Alcon Standard Operating Procedures (SOPs)
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Provide support in reconciliation activities and audit as required.
Evaluate and escalate potential safety issues to management.

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Alcon is an Equal Chance Employer and takes pride in maintaining a diverse workplace. 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.

📌 Associate I, Patient Safety And Experience Bengaluru (India)
🏢 Alcon Research
📍 India