Pharmacovigilance Configuration Analyst

English
₹15000/MONTH
1 Year
Bachelor's (Preferred)
Work From Office
Apply now
Date Posted

11-Jul-2026

Location

Delhi (DL), 1

Job Type

Full Time

Company

Huntsman

Description

???? Job Title: PV System Configuration Analyst

???? Location: India
???? Job Type: Permanent


???? Main Responsibilities:

  • Manage PV Configuration Standards, including:

    • Distribution Rules

    • Study Configurations in LSMV, LSR, and EV Triage modules

  • Handle PV system configurations for:

    • Company Products

    • Clinical & Post-Marketed Studies

    • Business User Roles & Data Privacy

    • Code Lists, Libraries, MedDRA, WHO

    • Distribution Rules, Accounts & HA Destinations

    • E2B Profiles, SDEA Profiles & Gateways

  • Maintain E2B Gateways with Health Authorities and Business Partners

  • Support Data Migration and Ingestion Requests

  • Perform User Acceptance Testing (UAT) for configuration changes

  • Document configuration changes in collaboration with business users

  • Facilitate training sessions and update training materials

  • Provide Safety Data and Ad-hoc Reports during audits and inspections

  • Collaborate with digital vendor teams for configuration changes, testing, and deployments

  • Work in an Agile environment


????‍???? Experience Required:

  • 6–8 years in the pharmaceutical industry, particularly with GxP systems

  • Proven background in:

    • Pharmacovigilance system operations

    • PV Databases (e.g., Argus, Aris-G, VAULT Safety, LSMV)

    • Configuration management and documentation

    • IS and validation processes

    • Safety reporting compliance (CIOMS, EudraVigilance, FDA REMS)

  • Proficient in:

    • SQL / PL-SQL

    • Microsoft Office (Excel, Word, PowerPoint)

    • Business Intelligence Tools: Power BI, Spotfire


???? Knowledge & Skills:

  • Familiar with ICH GVP, GxP, and regulatory safety requirements

  • Experience with UAT, system upgrades, and data migration

  • Cross-functional communication with Clinical, Regulatory, and Medical Affairs teams

  • Process Improvement experience is a plus


???? Soft Skills:

  • Strong stakeholder management, negotiation, and global collaboration skills

  • High attention to detail, analytical thinking, and problem-solving abilities

  • Excellent organizational and project management capabilities

  • Effective communicator across multicultural environments

  • Team player with strategic leadership potential


???? Education & Language:

  • Bachelor's in Pharmacy / Life Sciences / Engineering (or equivalent)

  • Fluency in English (verbal and written)


This role is a strategic opportunity for experienced professionals in pharmacovigilance systems who want to contribute to global drug safety compliance through expert configuration and data management practices.

4o

 



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