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Amarant Lifesciences Hiring for Pharmacovigilance

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Amarant Lifesciences Private Limited has announced new openings for Executive / Senior Executive / Specialist – Pharmacovigilance professionals in Delhi / NCR. This opportunity is ideal for candidates with 1–5 years of pharmacovigilance or drug safety experience looking to work in a global regulatory and consulting environment.

The role involves end-to-end pharmacovigilance activities, including ICSR processing, literature surveillance, regulatory submissions, and audit support, ensuring compliance with global drug safety regulations such as ICH, GVP, USFDA, EMA, and MHRA.

If you are actively searching for pharmacovigilance jobs in India, drug safety executive roles, or ICSR processing jobs, this position offers strong career growth and exposure to international PV projects.

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Key Responsibilities – Pharmacovigilance Role

  • Perform end-to-end ICSR processing from spontaneous, clinical, literature, and solicited sources
  • Case intake, triage, data entry, MedDRA & WHO-DD coding, narrative writing, QC, and follow-ups
  • Conduct systematic literature surveillance and generate compliant literature ICSRs
  • Ensure timely regulatory submissions to global health authorities (USFDA, EMA, MHRA, PMDA, etc.)
  • Support aggregate safety reports such as PSUR/PBRER and DSUR
  • Maintain compliance with global PV regulations, internal SOPs, and client procedures
  • Support internal, client, and regulatory audits, including CAPA implementation
  • Assist in signal detection and safety data review activities
  • Perform regulatory intelligence monitoring
  • Collaborate with cross-functional and client teams in a consulting setup

Eligibility Criteria & Qualifications

Education

  • Graduate or Postgraduate in Life Sciences
    (B.Pharm, M.Pharm, Biotechnology, Biology, Chemistry, or related fields)
  • Master’s degree preferred

Experience

  • 1–5 years of experience in Pharmacovigilance / Drug Safety

Technical Skills

  • Hands-on experience with safety databases such as Argus, ArisG, Veeva, or similar
  • Strong knowledge of global pharmacovigilance regulations
  • Excellent communication, analytical, and documentation skills

Why Join Amarant Lifesciences?

  • Exposure to global pharmacovigilance projects
  • Strong learning environment with regulatory and audit exposure
  • Career growth in drug safety and regulatory compliance
  • Collaborative consulting culture
  • Permanent, full-time opportunity in a growing life sciences organization

Job Details at a Glance

  • Job Title: Executive / Sr. Executive / Specialist – Pharmacovigilance
  • Company: Amarant Lifesciences Private Limited
  • Location: Delhi / NCR
  • Experience Required: 1–5 Years
  • Employment Type: Full Time, Permanent
  • Openings: 2
  • Industry: Pharmaceutical & Life Sciences

How to Apply

Application Link

Amarant Lifesciences Hiring for Pharmacovigilance

Email id: info@amarantls.com

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