Join GSK’s Pharmacovigilance Excellence Team in Bengaluru!
Are you a passionate and detail-oriented individual looking to contribute to global health and drug safety? GSK, a leading global biopharmaceutical company, is seeking talented individuals to join our Pharmacovigilance (PV) Excellence team in Bengaluru. We are currently hiring for two positions: Technical Associate Intern and Technical Associate II.
These roles offer an exciting opportunity to contribute to the advancement of drug safety, PV operations, safety systems, and regulatory support. Whether you’re a recent graduate with a background in Health Sciences or an experienced professional in Pharmacovigilance, we encourage you to apply and be a part of our mission to improve the quality of human life.
Read on to learn more about each position and how to apply.
1. Technical Associate Intern – PV Excellence
Location: Bengaluru – Luxor North Tower
Experience: Entry-Level (Bachelor’s in Health Sciences)
Department: PV Excellence (PVE)
Type: Full-time
About the Role:
As a Technical Associate Intern in PV Excellence, you will play a crucial supporting role in ensuring the safety and efficacy of our pharmaceutical products. This role provides a fantastic opportunity to learn and develop within a dynamic and highly regulated environment. You will be exposed to a wide range of PV activities, gaining valuable experience in various aspects of drug safety and regulatory compliance.
Key Responsibilities:
- Provide cross-enterprise technical support within the PV Excellence department.
- Assist Global Process Owners (GPOs) and Subject Process Leads (SPLs) in various PV process activities.
- Manage and maintain PV documentation using Veeva Vault (Regulatory & Clinical).
- Assist in the collection, compilation, and reporting of key performance metrics.
- Support Management Monitoring activities and daily mailbox triage.
- Maintain and update PVE webpages, documentation repositories, and provide eTMF support.
- Assist in activities related to Medical Device safety, Case Awareness Tool, Terms of Interest (TOI), MedDRA coding, and Targeted Follow-up Questions (TFQs).
- Support Safety Communications and Development Core Safety Information updates.
Required Qualifications:
- Bachelor’s degree in Health Sciences or a related field.
- Excellent communication skills with fluency in English, both written and verbal.
- Strong computer skills, including proficiency in Microsoft Word and Excel, and experience with document management systems.
- Familiarity with scientific and medical terminology is preferred.
- Demonstrated ability to work under pressure and meet deadlines.
2. Technical Associate II – PV Excellence
Location: Bengaluru – Luxor North Tower
Experience: 2–4 years
Department: PV Excellence (PVE)
Type: Full-time
About the Role:
As a Technical Associate II in PV Excellence, you will leverage your experience to contribute to the efficient and compliant management of PV documentation and processes. This role offers the opportunity to contribute to continuous improvement initiatives and act as a subject matter expert for document management systems. You will play a vital role in supporting signal detection activities and ensuring compliance with global PV regulations.
Key Responsibilities:
- Serve as the Template Manager for PV documentation within Veeva Vault.
- Support interactions with third-party vendors regarding Aggregate Reports.
- Manage the collection, reporting, and analysis of key performance metrics, and support Management Monitoring.
- Manage access provisioning for various systems, including Submission Portals, Shared Drives, and Citrix.
- Contribute to process improvement initiatives to enhance efficiency and compliance.
- Serve as a Subject Matter Expert (SME) and business owner for document management systems.
- Support Signal Detection, Eudravigilance, Risk Management Plan (RMP), Post-Authorization Safety Studies (PASS), and Targeted Safety Surveillance (TSS) activities.
- Assist in activities related to Medical Device safety, eTMF support, and MedDRA coding.
- Manage updates for Reference Safety Information.
- Support training, inspections, and audits related to PV processes.
Required Qualifications:
- Bachelor’s degree in Health Sciences or a related discipline.
- 2–4 years of experience in Pharmacovigilance or Safety Operations.
- Strong understanding of global PV regulations (e.g., ICH, EU).
- Excellent technical and documentation skills, including experience with electronic document management systems.
- Knowledge of Clinical, Regulatory Affairs, and Safety Systems is preferred.
- Ability to work independently and adapt to evolving processes and regulations.
Why Join GSK?
- Impactful Work: Contribute to a world-leading biopharmaceutical company impacting global health.
- Innovation: Opportunity to innovate in PV Excellence, Drug Safety, and R&D systems.
- Culture: Inclusive, ethical, and supportive work environment.
- Growth: Career growth opportunities across global PV and safety operations.
How to Apply:
We are currently accepting applications for both the Technical Associate Intern and Technical Associate II positions. Don’t miss this opportunity to join our team and make a difference!