Associate I, Patient Safety and Experience
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Before you apply
LocationBangalore, India
Typefull-time
SeniorityEntry
Company size10,000+ people
PostedNov 3, 2026 · 2d ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
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
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
Maintains working knowledge of Alcon Products for assigned therapeutic areas
Maintains working knowledge of eye anatomy
Maintains working knowledge of common diseases
Maintains working knowledge of ophthalmic evaluation procedures
Maintains working knowledge of eye terminology and abbreviations
Maintains working knowledge of safety database(s) and reporting tools
Process and review Surgical – Intra Ocular Lens (IOL) complaint records in accordance with Alcon SOPs
Provide support in reconciliation activities and audit as required
Evaluate and escalate potential safety issues to management
Adherence to all corporate compliance guidelines & corporate programs
About the role
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.
Responsibilities
•
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 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.