Elanco is hiring for the position of Product Safety Manager – Signal Detection and Data Assembly Team within its Global Pharmacovigilance (PV) team. The opportunity is available in Bangalore, India, along with Warsaw, Poland, and Lisbon, Portugal.
The role focuses on pharmacovigilance literature surveillance, safety data evaluation, signal detection, aggregate report preparation, and benefit-risk assessments. Candidates with a pharmacy, veterinary medicine, or life sciences background and 1–3 years of industry experience in pharmacovigilance or medical writing are eligible to apply.
Elanco Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Elanco |
| Job Position | Product Safety Manager |
| Team | Signal Detection and Data Assembly |
| Department | Global Pharmacovigilance |
| Job Location | Bangalore, India |
| Other Locations | Warsaw, Poland; Lisbon, Portugal |
| Experience | 1–3 Years |
| Employment Type | Full Time |
| Qualification | Veterinary Medicine, Pharmacy or Life Sciences |
| Job Requisition ID | R0027318 |
| Travel Requirement | Up to 10% annually |
| Application Mode | Online |
Positions
Product Safety Manager – Signal Detection and Data Assembly Team
The selected candidate will support global pharmacovigilance activities, including scientific literature surveillance, safety data analysis, signal detection, aggregate reporting, and regulatory safety documentation for non-High Profile Products (non-HPPs).
Key Responsibilities
- Conduct literature surveillance and critical reviews to support signal detection, safety monitoring, and aggregate report preparation.
- Identify, evaluate, and document safety information from scientific and medical literature.
- Assess and communicate adverse event reports and emerging safety concerns.
- Support benefit-risk evaluations through the analysis and interpretation of published safety data.
- Collaborate with cross-functional stakeholders on safety assessments and regulatory reporting.
- Author and review aggregate reports and regulatory safety documents, including Annual Signal Management Reports and Benefit-Risk Safety Reports.
- Manage Veeva Vault RIM activities and workflows.
- Coordinate with Regulatory Affairs, PV Affiliates, and other functional teams to collect relevant safety information.
- Maintain pharmacovigilance documentation and records in an inspection- and audit-ready state.
- Support regulatory inspections and audits when applicable.
Eligibility Criteria and Qualifications
Candidates applying for the Elanco Product Safety Manager position should meet the following requirements:
Educational Qualification:
- Graduation in Veterinary Medicine.
- Post-graduation in Pharmacy.
- Any other Life Sciences background.
Experience:
- 1–3 years of industry experience in Pharmacovigilance (PV) or Medical Writing.
Required Skills
- Excellent written and verbal communication skills.
- Ability to communicate technical and logical information with global stakeholders.
- Strong knowledge of Microsoft Office applications.
- In-depth knowledge of GxP requirements and regulatory guidelines.
- Understanding of operational Regulatory and R&D principles.
- Knowledge of medical terminology and clinical concepts relevant to adverse event case reporting.
- Understanding of aggregate report requirements and report types.
- Ability to work independently and collaborate with global teams across different time zones.
- Experience with electronic document management systems such as Veeva Vault.
- Knowledge of document templates, styles, and submission-ready formatting.
Preferred Qualifications
Elanco gives preference to candidates with:
- Understanding of aggregate safety reporting requirements.
- Experience with Veeva Vault or similar electronic document management systems.
- Knowledge of medical literature review and safety data assessment.
- Ability to prepare and review regulatory safety documents.
