Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate I, Patient Safety & Experience (Non-Md)

Alcon
Alcon
1-2 years
₹3.5–5.5 LPA
10 July 26, 2025
Job Description
Job Type: Full Time Education: Optometry/M. Pharm/B. Pharm /BDS/BAMS/BHMS/B.Tech/ Registered Nurse Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate I, Patient Safety & Experience (Non-MD) – Alcon
Location: Bengaluru, Karnataka
Work Mode: On-site | Full-time
Estimated Salary: ₹3.5–5.5 LPA (based on experience and industry averages)


Job Purpose:
Support day-to-day vigilance activities by processing quality and adverse event complaints related to Alcon-manufactured products, ensuring compliance with international medical device regulations and internal SOPs.


Key Responsibilities:

Case Processing & Documentation:

  • Manage case files per SOPs; perform initial and follow-up data assessments.

  • Communicate with affiliate offices to obtain complete case data.

  • Assign appropriate product and event codes in safety databases.

  • Prepare quality reports for submission to Health Authorities and internal QA teams.

  • Launch investigations for product complaints and safety-related concerns.

Safety & Regulatory Support:

  • Conduct device vigilance activities in compliance with local and global regulations.

  • Perform reconciliation and audit support tasks as needed.

  • Escalate safety signals to management and maintain updated knowledge on assigned therapeutic areas.

Knowledge Maintenance:

  • Understand Alcon products, eye anatomy, ophthalmic diseases, procedures, and related documentation.

  • Use relevant databases and tools for case coding and safety reporting.


Key Performance Indicators (KPIs):

  • Timely and accurate case closures and regulatory report submissions.

  • Compliance with internal quality standards.

  • High-quality documentation aligned with global regulatory timelines.


Ideal Candidate Profile:

Education:

  • Minimum: Bachelor’s degree in Science

  • Preferred: Degree in Optometry, Pharmacy (B.Pharm/M.Pharm), BDS, BAMS, BHMS, Biomedical Engineering, or as a Registered Nurse

Experience:

  • Minimum: 1–2 years in a healthcare-related field

  • Preferred: Experience in Device Vigilance, Pharmacovigilance, Clinical Research, Medical Coding, or Regulatory Submissions

Skills:

  • Strong decision-making, communication, and multitasking skills

  • Basic understanding of device safety regulations

  • Proficient in MS Office

  • Fluent in English (written & spoken)


About Alcon:
Alcon is a global leader in eye care, committed to helping people see brilliantly. The company offers a diverse and inclusive environment, encouraging growth and collaboration across roles and functions.