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Apply Now: Pharmacovigilance & Scientific Writing Jobs at Opella Healthcare

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Opella is a global leader in self-care and OTC (Over-The-Counter) healthcare, with a strong portfolio of well-known brands like Allegra, Buscopan, Doliprane, and Dulcolax. With 11,000+ employees worldwide, 13 manufacturing sites, and 4 innovation centers, Opella is committed to making healthcare simple and accessible.

As a B Corp-certified company, Opella focuses on sustainable healthcare solutions while fostering an inclusive, innovative work culture.

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Job Openings at Opella Hyderabad

1. Junior Scientific Writer

📍 Location: Hyderabad
📅 Last Date to Apply: July 31, 2025
🔗 Requisition ID: R2799591

Job Description:

  • Develop scientific & medical content (manuscripts, abstracts, slide decks).
  • Support publication & medical education projects.
  • Collaborate with healthcare professionals & cross-functional teams.
  • Ensure compliance with PromoMats/iEnvision documentation.

Eligibility:

  • Advanced degree (Life Sciences/Pharmacy/Medicine).
  • 0-2 years in medical/scientific writing.
  • Strong English communication & stakeholder management skills.

2. Pharmacovigilance Case MR Oversight Specialist

📍 Location: Hyderabad
📅 Last Date to Apply: August 31, 2025
🔗 Requisition ID: R2804114

Job Description:

  • Perform medical review of ICSRs (Individual Case Safety Reports).
  • Ensure timely & accurate safety data processing in PV databases (ARGUS, Aris-G).
  • Support signal detection, risk management plans (RMPs), and regulatory submissions.
  • Oversee vendor case processing & quality checks.

Eligibility:

  • MBBS/MD/PharmD with 2-3 years in ICSR medical review.
  • Experience in PV databases, labelling, causality assessment.
  • Strong regulatory knowledge (FDA, EMA, ICH-GVP).

3. Pharmacovigilance Product & Regulatory Associate

📍 Location: Hyderabad
📅 Last Date to Apply: August 5, 2025
🔗 Requisition ID: R2804117

Job Description:

  • Manage PV product configurations & reporting rules in safety databases.
  • Coordinate with Country Safety Heads (CSHs) & QPPV office.
  • Ensure compliance with global PV regulations.
  • Maintain Veeva Vault labelling documents.

Eligibility:

  • Bachelor’s in Pharmacy/Life Sciences + 3-4 years in PV case management.
  • Experience in PV databases (ARGUS, Aris-G, Veeva Vault).
  • Strong regulatory & compliance knowledge.

Why Join Opella?

✅ Challenging & Purposeful Work – Impact global healthcare.
✅ Inclusive & Collaborative Culture – Work with diverse teams.
✅ Career Growth – Develop skills in pharma, PV, and medical writing.
✅ B Corp Certified – Ethical, sustainable workplace.


How to Apply?

Application Link For Junior Scientific Writer

Application Link For Pharmacovigilance Case MR Oversight Specialist

Application Link For Pharmacovigilance Product & Regulatory Associate

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