Pharmacovigilance Specialist Hiring at Opella Healthcare

Pharmacovigilance Specialist – B.Pharm/Life Sciences | Hyderabad

Apply now for Pharmacovigilance Reporting & Analytics Specialist at Opella, Hyderabad. B.Pharm/Life Sciences graduates with 5+ years’ experience preferred.

Opella is hiring a Pharmacovigilance Reporting and Analytics Specialist in Hyderabad. If you’re passionate about drug safety, regulatory compliance, and advanced reporting systems, this is your opportunity to join a global leader in the OTC and VMS healthcare market. With over 100 consumer-loved brands and a presence across 100+ countries, Opella empowers professionals to drive meaningful impact in healthcare.

Company Overview

Opella is a globally recognized self-care challenger headquartered in France, known for its strong presence in the Over-The-Counter (OTC) and Vitamins, Minerals & Supplements (VMS) market. With 11,000+ employees, 13 manufacturing sites, and 4 specialized science centers, Opella is the proud maker of brands such as Allegra, Dulcolax, Buscopan, Enterogermina, Essentiale, Doliprane, and Mucosolvan. Being B Corp certified, the company is committed to sustainability and improving health outcomes for millions of consumers worldwide.

Job Role & Responsibilities

As a Pharmacovigilance Reporting and Analytics Specialist, you will:

• Design, develop, test, and deploy safety compliance and reporting solutions.
• Collaborate with digital vendor teams for compliance reports and dashboards.
• Analyze case submission delays, propose corrective actions (CAPAs), and ensure timely resolutions.
• Maintain validation of safety reports generated from LSRA.
• Provide oversight reports for QPPV office.
• Support audits, inspections, and ad-hoc safety reporting requirements.
• Participate in automation of PV reports using Power BI and dashboarding tools.
• Manage incident handling, system upgrades, and change management activities.
• Ensure compliance with global PV regulations and standards.
• Contribute to continuous improvement in pharmacovigilance systems and reporting efficiency.

Eligibility / Qualifications

• Education: Bachelor’s degree in Pharmacy, Life Sciences, Engineering or equivalent.
• Experience: Minimum 5 years in pharmaceutical industry with focus on pharmacovigilance reporting.
• Technical Skills:
  • PV Databases: ARGUS, Aris-G (LSMV), LSRA.
  • Reporting Tools: Cognos, Power BI (developer-level proficiency).
  • Programming: Python, R, JavaScript.
  • Database Management: SQL, PL/SQL, Power BI DAX.
  • Knowledge of AI/ML, NLP modules preferred.
• Soft Skills:
  • Strong stakeholder management and negotiation.
  • Excellent written and verbal communication.
  • Effective teamwork in cross-functional, multicultural settings.
  • Problem-solving, analytical, and project management skills.

Location & Salary

• Location: Hyderabad, India
• Work Mode: On-site, Full-time
• Salary: Competitive, aligned with experience and industry standards.

Application Process

Interested candidates can apply directly through the official listing:
👉 Apply Here

Apply before the role closes to secure your spot!

Why Join Opella?

• Opportunity to work with global PV systems and compliance tools.
• Be part of a mission-driven organization improving self-care worldwide.
• Work culture based on collaboration, courage, and simplicity.
• Growth opportunities in drug safety, compliance, and data analytics.
• Inclusive, supportive, and innovation-driven work environment.

FAQs

Q1: What is the required qualification for this role?
A Bachelor’s degree in Pharmacy, Life Sciences, or Engineering is required.

Q2: How much experience is needed?
A minimum of 5 years in pharmacovigilance reporting or compliance systems.

Q3: Which tools should candidates know?
Proficiency in Power BI, Cognos, SQL/PLSQL, ARGUS, and Aris-G is essential.

Q4: Is this role hybrid or on-site?
This is a full-time on-site role in Hyderabad.

Q5: Does the role involve global exposure?
Yes, candidates will support global PV compliance and reporting operations.

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