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Soterius Hiring for Pharmacovigilance and Drug Safety professionals in Mumbai & Noida

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Soterius

Degree in Pharmacy, Pharm D, BHMS, BDS or equivalent qualification.

Mumbai / Noida

2 - 6 Years+

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Soterius is hiring experienced Pharmacovigilance and Drug Safety professionals for two case processing positions in Mumbai and Noida. The current openings include Team Lead โ€“ Case Processing and Senior PV Scientist โ€“ Case Processing.

These Soterius pharmacovigilance jobs offer opportunities for professionals with experience in ICSR case processing, MedDRA coding, narrative writing, quality review, E2B submissions, safety databases, GVP compliance, and consumer healthcare pharmacovigilance.

Candidates looking for pharmacovigilance jobs in Mumbai, drug safety jobs in Noida, ICSR case processing jobs, Senior PV Scientist jobs, or PV Team Lead jobs can review the eligibility criteria below.

Soterius Job Openings 2026

ParticularTeam Lead โ€“ Case ProcessingSenior PV Scientist โ€“ Case Processing
CompanySoteriusSoterius
DepartmentPharmacovigilance / Case ProcessingPharmacovigilance / Case Processing
PositionTeam Lead โ€“ Case ProcessingSenior PV Scientist โ€“ Case Processing
Experience6+ Years2+ Years
LocationMumbai / NoidaMumbai / Noida
EmploymentFull-TimeFull-Time
IndustryPharmacovigilance / Drug SafetyPharmacovigilance / Drug Safety

1. Team Lead โ€“ Case Processing

Soterius is looking for an experienced Team Lead โ€“ Case Processing to manage pharmacovigilance case processing operations within a high-volume OTC and consumer healthcare safety program.

The selected professional will report to the Case Management Lead and oversee an operational team working across the complete ICSR lifecycle, including intake, triage, processing, submission and quality control.

Key Responsibilities

  • Lead the pharmacovigilance case processing team and manage daily workload allocation.
  • Monitor team productivity, quality and compliance across the case lifecycle.
  • Oversee case intake, book-in, triage and case validity assessment.
  • Supervise ICSR data entry, MedDRA coding and narrative writing.
  • Oversee E2B submissions and safety gateway operations.
  • Manage EudraVigilance downloads and pharmacovigilance mailbox activities where assigned.
  • Perform and supervise inline quality control activities.
  • Monitor case processing errors, trends and QC metrics.
  • Ensure cases are processed and submitted within applicable compliance timelines.
  • Handle operational escalations and case processing issues.
  • Manage employee performance, training and professional development.
  • Maintain inspection readiness.
  • Support internal and external audits and regulatory inspections.

Qualification & Experience

Candidates should have:

  • Degree in Pharmacy, Pharm D, BHMS, BDS or equivalent qualification.
  • Minimum 6+ years of relevant experience.
  • Experience in pharmacovigilance, drug safety or allied clinical/scientific/safety domains.
  • Strong understanding of end-to-end ICSR case processing.
  • Experience managing or leading pharmacovigilance operations is highly relevant.

Required Skills

  • Pharmacovigilance case processing
  • ICSR processing
  • Case intake and triage
  • Validity assessment
  • MedDRA coding
  • Narrative writing
  • E2B submissions
  • Gateway operations
  • EudraVigilance
  • Inline QC
  • Error trend analysis
  • Team management
  • Workload management
  • Compliance management
  • Consumer healthcare pharmacovigilance
  • Safety database experience with LSMV, Oracle Argus, Veeva or equivalent systems

2. Senior PV Scientist โ€“ Case Processing

The Senior PV Scientist โ€“ Case Processing position is suitable for experienced pharmacovigilance professionals with strong hands-on expertise in end-to-end ICSR processing, quality review and case submission.

The role also involves managing complex cases, maintaining GVP compliance and mentoring junior PV professionals.

Key Responsibilities

  • Perform senior-level end-to-end ICSR case processing.
  • Handle case intake, triage, data entry, submission and follow-up activities.
  • Own quality control of processed safety cases.
  • Monitor and maintain pharmacovigilance quality standards.
  • Perform and review MedDRA coding.
  • Prepare and review high-quality case narratives.
  • Manage complex, escalated and challenging safety cases.
  • Support aggregate reporting activities when required.
  • Provide support for signal management activities as applicable.
  • Mentor junior PV Scientists and associates.
  • Ensure compliance with applicable Good Pharmacovigilance Practices (GVP).
  • Maintain inspection readiness.
  • Support audits and inspections involving the case processing function.

Qualification & Experience

According to the provided Soterius job information, candidates should have:

  • 2+ years of relevant experience in pharmacovigilance, drug safety, or an allied clinical, scientific or safety domain.
  • Strong hands-on knowledge of end-to-end case processing.
  • Experience with ICSR quality review and case submission.
  • Knowledge of safety databases such as Oracle Argus, LSMV, Veeva or equivalent systems.
  • Knowledge of MedDRA terminology and narrative writing.
  • Understanding of GVP requirements.

Note: A specific educational qualification was not stated in the provided Senior PV Scientist job description. Candidates should verify the complete eligibility requirements on the official Soterius career portal before applying.


Skills That Can Strengthen Your Application

Candidates with practical exposure to the following areas may be particularly relevant for these Soterius pharmacovigilance jobs:

ICSR Processing | Argus Safety | Veeva Safety | LSMV | MedDRA | Narrative Writing | Case Triage | Case Validity | E2B(R3) | EudraVigilance | Case Submission | Quality Control | GVP | Drug Safety | Consumer Health Pharmacovigilance


Why Consider These Soterius PV Roles?

These positions provide experienced pharmacovigilance professionals an opportunity to work across important components of the safety case lifecycle.

Potential professional exposure includes:

  • End-to-end ICSR case management
  • High-volume consumer healthcare pharmacovigilance
  • Safety database operations
  • Regulatory case submissions
  • Quality review and compliance
  • Audit and inspection readiness
  • Complex case handling
  • Team mentoring and leadership
  • International pharmacovigilance processes

The Team Lead opening is particularly relevant for professionals looking to progress into pharmacovigilance operations leadership, while the Senior PV Scientist position may suit candidates seeking deeper technical ownership of ICSR processing and quality review.


Estimated Salary

Soterius has not disclosed compensation in the job description provided.

For structured-data purposes only, a reasonable market-based estimate may be:

PositionEstimated Annual Salary
Senior PV Scientist โ€“ Case Processingโ‚น5,00,000 โ€“ โ‚น10,00,000
Team Lead โ€“ Case Processingโ‚น9,00,000 โ€“ โ‚น16,00,000

How to Apply

Application Link For Team Lead โ€“ Case Processing

Application Link For Senior PV Scientist โ€“ Case Processing

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