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Risk Evidence Writer Job at Reckitt | Regulatory Medical Writing

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Reckitt, a global leader in consumer health and FMCG products, is hiring a Risk Evidence Writer in Gurugram for professionals with strong regulatory medical writing and pharmacovigilance experience. This role is ideal for candidates who specialize in benefitโ€“risk assessment, safety evidence synthesis, and scientific literature evaluation across medicines, medical devices, and consumer health products.

If you are seeking a regulatory medical writing job in Gurugram with strong growth potential and global exposure, this opportunity offers a dynamic environment to work on safety risk management, signal detection, and regulatory submissions.


๐Ÿ”น Position Details

  • Job Title: Risk Evidence Writer
  • Company: Reckitt
  • Location: Gurugram, Haryana
  • Experience Required: 3โ€“8 years
  • Employment Type: Full-time, Permanent
  • Industry: FMCG / Consumer Health
  • Department: Research & Development

๐Ÿ”น Key Responsibilities

  • Develop high-quality, accurate, and balanced scientific evidence review documents.
  • Support benefitโ€“risk strategies and safety risk minimization activities.
  • Conduct and manage systematic literature searches using MeSH and Emtree.
  • Critically appraise scientific data and synthesize safety conclusions.
  • Produce safety reports and position statements for RMPs, CCDS, and regulatory submissions.
  • Support global signal management and escalation of emerging safety signals.
  • Collaborate with Regulatory Affairs, Pharmacovigilance, and cross-functional teams.
  • Contribute to deployment and maintenance of signal detection systems and protocols.

๐Ÿ”น Qualifications & Experience

  • Bachelorโ€™s degree in a scientific discipline (postgraduate qualification preferred).
  • 3โ€“8 years of experience in pharmacovigilance, product safety, or regulatory medical writing.
  • Strong understanding of global medicines and medical device regulations.
  • Proven ability to critically analyze scientific and clinical data.
  • Excellent scientific writing, communication, and organizational skills.
  • Experience across multiple therapeutic areas is an advantage.

๐Ÿ”น Key Skills

  • Regulatory Medical Writing
  • Pharmacovigilance & Signal Management
  • Literature Search & Evidence Synthesis
  • Benefitโ€“Risk Assessment
  • Safety Documentation
  • Scientific Communication
  • Project Management

๐Ÿ”น Why Join Reckitt?

  • Global exposure to consumer health and regulated products.
  • Competitive compensation and benefits.
  • Opportunities for career growth in regulatory affairs and pharmacovigilance.
  • Collaborative, innovation-driven work culture.

๐Ÿ”น Estimated Salary Range (India)

โ‚น8,00,000 โ€“ โ‚น15,00,000 per annum (based on experience and industry benchmarks)


๐Ÿ”น How to Apply

Application Link

Risk Evidence Writer Job at Reckitt | Regulatory Medical Writing

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