Join Unilever’s Global Regulatory Affairs team in Bangalore for pharmacovigilance roles focused on consumer safety. Ideal entry-level position in post-market surveillance with US timezone overlap. Apply by Dec 31, 2025.
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About the Company
Unilever is a leading global consumer goods company with iconic brands in nutrition, personal care, hygiene, and wellbeing. Headquartered in London, Unilever operates in over 190 countries, employing diverse talent to drive sustainable innovation.
The R&D Bangalore center excels in scientific advancements for consumer healthcare and regulatory compliance.
Committed to equality, diversity, and inclusion, Unilever fosters an empowering environment for all employees. The company prioritizes consumer safety, ethical practices, and impactful careers in a dynamic, purpose-driven culture.
Job Details
- Company Name: Unilever
- Experience: 0-2 years
- Qualification: Bachelor’s or Master’s in Life Sciences, Pharmacy, or related field
- Location: Unilever R&D Bangalore, India
- Work Type: Full-time (requires significant US timezone overlap)
Job Description
Unilever seeks a detail-oriented Associate for Global Market Vigilance (GMV) in the Wellbeing Collective.
This entry-level pharmacovigilance role ensures post-market safety surveillance for consumer healthcare products. Candidates gain hands-on experience in adverse event management and regulatory compliance.
Associate, Global Market Vigilance (GMV)
- Department: Global Regulatory Affairs (GRA), Wellbeing Collective
- Location: Bangalore
- Role: Associate (Individual Contributor)
- Experience: 0-2 years in post-market safety/pharmacovigilance
- Education/Qualification: Bachelor’s/Master’s in Life Sciences, Pharmacy, or related
Skills/Qualifications
- Degree in Life Sciences, Pharmacy, or equivalent field
- Hands-on experience with scientific databases
- Foundational knowledge of post-market safety processes
- Strong diligence and organizational abilities
- Effective communication and documentation skills
- Proactive, collaborative team player
- Ability to thrive in fast-paced, cross-functional settings
Key Responsibilities
- Intake, triage, and document adverse events in Veeva Vault Safety
- Perform duplicate checks on AE cases
- Escalate serious cases promptly to management
- Gather complete information from internal/external partners
- Assist in narratives, causality assessments, and submissions
- Ensure timely compliance with global reporting requirements
- Maintain records and support archiving
- Aid in safety database configuration and validation
- Coordinate with Regulatory, QA, and R&D teams
- Track CAPAs and perform data reconciliations
- Contribute ideas for process improvements
Benefits/Perks
- Global exposure in consumer healthcare innovation
- Commitment to equality, diversity, and inclusion
- Professional development in pharmacovigilance
- Purpose-driven culture impacting consumer wellbeing
- Supportive environment for work-life balance
- Opportunities to collaborate across functions
- Focus on ethical, sustainable practices
How to Apply
Apply online through the official Unilever careers portal:
Job Requisition ID: R-1170195
Application deadline: December 31, 2025.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Unilever Career page.
Note: Official offers come only via Unilever’s Applicant Tracking System (ATS). Verify sources to avoid fraud.
For more regulatory affairs and pharmacovigilance opportunities, visit Pharma Recruiter. Advance your career in consumer safety — apply today!
Why You Should Join
Unilever offers an inclusive culture where diversity drives innovation and impact. Employees contribute to meaningful consumer safety in global wellbeing products. With strong emphasis on equality and professional growth, Unilever supports fulfilling careers.
This role provides entry-level access to pharmacovigilance expertise in a collaborative R&D environment. Join a company committed to sustainable, ethical practices and employee development.
FAQs
What qualifications are required for this GMV Associate role?
Bachelor’s/Master’s in Life Sciences/Pharmacy with 0-2 years in pharmacovigilance and database experience.
Does this position require specific working hours?
Yes, significant overlap with US time zones to support related businesses.
How do I apply safely for this Unilever job?
Use the official careers link or ATS; beware of unofficial offers which may be fraudulent.
What career growth can I expect?
Opportunities in global regulatory affairs, consumer safety, and cross-functional collaboration in a diverse, innovative company.