Health Science Job at GSK – Technical Associate Role
Explore a rewarding health science job with GSK as a Technical Associate II (PV Excellence) at the Bengaluru Luxor North Tower office. This role offers the chance to support global pharmacovigilance operations, contribute to safety excellence, and grow within one of the most trusted names in healthcare innovation. If you’re aiming for impactful GSK careers and the opportunity to make a meaningful difference, this position offers a strong pathway for advancement within GSK Jobs.
- Job Title: Technical Associate II (PV Excellence)
- Location: GSK Bengaluru Luxor North Tower
- Time Type: Full time
- Posted on: Posted Today
- Time Left to Apply: End Date: November 29, 2025 (7 hours left to apply)
- Job Requisition ID: 430868
About the Company
GSK is a world-leading biopharmaceutical company dedicated to improving the health of 2.5 billion people by the end of the decade. Known globally for innovation, GSK Careers offer opportunities that combine science, technology, and talent to advance healthcare. Through its ambitious R&D initiatives, GSK focuses on vaccines, medicines, and safety processes that shape the future of global health—making it an ideal destination for professionals seeking long-term growth through GSK Jobs.
Health Science Job – Education Requirements:
Bachelor’s degree in health sciences or related disciplines. Familiarity with medical/scientific industry desirable. Basic understanding of medically oriented tasks and technical support skills.
Job-Related Experience:
- 2–4 years of relevant experience.
- Fluent in English with strong communication skills.
- Excellent computer skills (Word, Excel, Internet/Intranet, document management systems).
- Familiarity with medical/scientific terminology desirable.
- Working knowledge of R&D organization preferred.
Job Purpose
This health science job involves providing enterprise-wide technical support within PV Excellence (PVE) and supporting the business across pharmacovigilance operations. The role supports Global Process Owners (GPOs) and Safety Process Leads (SPLs) with strategic oversight, ensuring compliant and efficient safety processes aligned with global PV regulations-an essential function within GSK Careers.
Health Science Job – Key Responsibilities:
- Act as Template Manager to support PV documentation in Veeva Vault (Regulatory and Clinical).
- Support interaction between PVE and third-party vendor activities for Aggregate Report management.
- Provide support for metric collection, compilation, and reporting.
- Assist with Management Monitoring activities.
- Manage access (Submission Portal, Aggregate Report shared drive, Group Management Portal, Citrix).
- Daily triage and management of group mailboxes.
- Contribute to process improvement initiatives.
- Act as Subject Matter Expert when required.
- Serve as business owner for document management systems.
- Review and maintain content on PVE-owned webpages to ensure accuracy and functionality.
- Support signal detection activities, including CVW and EMA publication reviews for signal-related data.
- Assist with Eudravigilance activities.
- Support RMP and Targeted Safety Study (TSS)/Post Approval Safety Study (PASS) activities, including RMP coordination.
- Provide support for eTMF and Medical Devices.
- Assist with Case Awareness Tool, Autolistedness profile, TOI, MedDRA, and TFQs.
- Oversee local Reference Safety Information updates and address related queries.
- Support Development Core Safety Information management.
- Assist with Safety Communications processes.
- Provide support for training, inspections, and audits.
Expected Competencies:
- Excellent organizational skills.
- Ability to work under pressure with tight deadlines while maintaining accuracy and integrity.
- Strong team player with effective communication skills (written and verbal).
- Ability to handle and escalate issues based on risk in a timely manner.
- Awareness of PV processes and global PV regulations.
- Preferred knowledge of process improvement techniques and ability to analyze performance metrics for continuous improvement.
- Preferred understanding of related disciplines (clinical, regulatory affairs, clinical statistics) relevant to aggregate report writing and clinical development.
- Ability to work independently, adapt to change, and maintain flexibility.
