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Manager (Medical Doctor), Global Market Vigilance (Gmv)

Unilever
Unilever
3+ years
Not Disclosed
10 Dec. 22, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Title: Manager (Medical Doctor) – Global Market Vigilance (GMV)
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Category: Pharmacovigilance / Research & Development

Company Overview:
Unilever’s Global Regulatory Affairs and Wellbeing Collective teams are committed to ensuring product safety and regulatory compliance across consumer healthcare and pharmaceutical products. The GMV team leverages clinical expertise, regulatory knowledge, and global pharmacovigilance practices to safeguard consumers and support internal stakeholders.

Role Overview:
We are seeking a Medical Doctor (MBBS/MD) with hands-on pharmacovigilance experience to serve as a Manager in Global Market Vigilance. This role involves in-depth adverse event (AE) review, medical case assessment, regulatory compliance, and cross-functional collaboration to ensure consumer safety.

Key Responsibilities:

Case Assessment & Medical Review:

  • Conduct detailed reviews of adverse events (AEs) and health-related complaints from consumers, healthcare professionals, and clinical studies.

  • Evaluate case seriousness, expectedness, and completeness, ensuring data integrity.

  • Accurately document and code AEs using MedDRA.

  • Analyze aggregate safety data to detect potential safety signals or trends.

Regulatory Compliance & Quality Assurance:

  • Ensure medical review and case processing comply with global and local regulations (e.g., FDA 21 CFR 312, EMA GVP) and internal SOPs.

  • Support internal and external audits as a subject matter expert on AE management.

Cross-Functional Collaboration:

  • Act as the key safety liaison for Legal, Marketing, R&D, and Quality Assurance teams.

  • Provide expert guidance on AE inquiries and risk assessment.

Mentorship & Continuous Improvement:

  • Mentor and train team members on AE assessment and medical review processes.

  • Identify workflow and process improvements to enhance compliance, accuracy, and efficiency.

Required Qualifications & Experience:

  • Medical degree (MBBS or MD) from an accredited institution.

  • Minimum 3 years of experience in pharmacovigilance, patient/consumer safety within Pharmaceutical, Medical Device, or Consumer Healthcare industries.

  • Hands-on experience with global PV databases; experience with Veeva Vault Safety is preferred.

  • Proficiency in safety and causality assessment, medical narrative writing, MedDRA coding, MedWatch, and CIOMS report review.

Skills & Competencies:

  • Strong clinical knowledge: human physiology, pharmacology, and adverse event interpretation.

  • In-depth understanding of global pharmacovigilance regulations and industry best practices.

  • Excellent analytical, critical thinking, and problem-solving skills.

  • Effective communication with scientific and non-scientific stakeholders.

  • Ability to mentor teams and improve processes.

Why Join Unilever:

  • Contribute to consumer safety on a global scale.

  • Collaborate with cross-functional teams in a fast-paced, regulated environment.

  • Participate in continuous learning and professional development opportunities.

Apply Now: Take the next step in your pharmacovigilance career as a Manager (Medical Doctor), Global Market Vigilance (GMV) at Unilever Bangalore.