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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.


Job Openings at Opella Hyderabad

1. Junior Scientific Writer

๐Ÿ“ Location: Hyderabad
๐Ÿ“… Last Date to Apply: July 31, 2025
๐Ÿ”— Requisition ID: R2799591

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Job Description:

  • Developย scientific & medical contentย (manuscripts, abstracts, slide decks).
  • Supportย publication & medical educationย projects.
  • Collaborate withย healthcare professionals & cross-functional teams.
  • Ensure compliance withย PromoMats/iEnvisionย documentation.

Eligibility:

  • Advanced degreeย (Life Sciences/Pharmacy/Medicine).
  • 0-2 yearsย in medical/scientific writing.
  • Strongย English communication & stakeholder managementย skills.

2. Pharmacovigilance Case MR Oversight Specialist

๐Ÿ“ Location: Hyderabad
๐Ÿ“… Last Date to Apply: August 31, 2025
๐Ÿ”— Requisition ID: R2804114

Job Description:

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

Eligibility:

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

3. Pharmacovigilance Product & Regulatory Associate

๐Ÿ“ Location: Hyderabad
๐Ÿ“… Last Date to Apply: August 5, 2025
๐Ÿ”— Requisition ID: R2804117

Job Description:

  • Manageย PV product configurations & reporting rulesย in safety databases.
  • Coordinate withย Country Safety Heads (CSHs) & QPPV office.
  • Ensureย compliance with global PV regulations.
  • Maintainย Veeva Vault labelling documents.

Eligibility:

  • Bachelorโ€™s in Pharmacy/Life Sciencesย +ย 3-4 years in PV case management.
  • Experience inย PV databases (ARGUS, Aris-G, Veeva Vault).
  • Strongย regulatory & compliance knowledge.

Why Join Opella?

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


How to Apply?

Application Link Forย Junior Scientific Writer

Application Link For Pharmacovigilance Case MR Oversight Specialist

Application Link For Pharmacovigilance Product & Regulatory Associate

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