GSK (GlaxoSmithKline), a global biopharma leader, is hiring for two major Pharmacovigilance (PV) Excellence roles in Bengaluru. These positions offer an excellent opportunity for freshers and experienced candidates looking to build a strong career in drug safety, PV operations, safety systems, and regulatory support.
If you’re looking for PV jobs in Bangalore, GSK careers 2025, or pharma technical associate openings, this detailed job article covers everything — responsibilities, qualifications, benefits, and how to apply.
1. Technical Associate Intern – PV Excellence (GSK)
Location: Bengaluru – Luxor North Tower
Experience: Freshers (Bachelor’s in Health Sciences)
Department: PV Excellence (PVE)
Type: Full-time
Key Responsibilities
- Provide cross-enterprise technical support within PV Excellence.
- Support GPOs and SPLs for PV process activities.
- Manage PV documentation using Veeva Vault (Regulatory & Clinical).
- Assist in metric collection, compilation, and reporting.
- Support Management Monitoring and daily mailbox triage.
- Maintain PVE webpages, documentation repositories, and eTMF support.
- Assist in Medical Device safety, Case Awareness Tool, TOI, MedDRA & TFQs.
- Support Safety Communications & Development Core Safety Information.
Required Qualifications
- Bachelor’s degree in Health Sciences or related field.
- Strong communication skills, fluent in English.
- Excellent computer skills (Word, Excel, document management systems).
- Familiarity with scientific/medical terminology (preferred).
- Ability to work under pressure and meet deadlines.
2. Technical Associate II – PV Excellence (GSK)
Location: Bengaluru – Luxor North Tower
Experience: 2–4 years
Department: PV Excellence (PVE)
Type: Full-time
Key Responsibilities
- Act as Template Manager for PV documentation in Veeva Vault.
- Support interactions with third-party vendors for Aggregate Reports.
- Handle metrics collection, reporting, and management monitoring.
- Manage access provisioning (Submission Portals, Shared Drives, Citrix).
- Contribute to process improvement initiatives.
- Serve as SME and business owner for document management systems.
- Support Signal Detection, Eudravigilance, RMP, PASS, TSS activities.
- Assist in Medical Device safety, eTMF support, MedDRA activities.
- Manage updates for Reference Safety Information.
- Support training, inspections, and audits.
Required Qualifications
- Bachelor’s in Health Sciences or related discipline.
- 2–4 years of Pharmacovigilance / Safety Operations experience.
- Strong understanding of global PV regulations.
- Excellent technical and documentation skills.
- Knowledge of Clinical, Regulatory Affairs, and Safety Systems (preferred).
- Ability to work independently and adapt to evolving processes.
Why Join GSK?
- Work with a world-leading biopharma company impacting global health.
- Opportunity to innovate in PV Excellence, Drug Safety & R&D systems.
- Inclusive, ethical, supportive work culture.
- Career growth across global PV and safety operations.
How to Apply
Application Link Technical Associate Intern
Application Link Technical Associate II
11 Hours left to apply
