Digital Quality Expert

Opella · Hyderabad, India

Hyderabad, India10–12 yearsPosted 2 Nov 2026Last checked 14 Nov 2026

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About the role

Job title: Digital Quality Expert Location: Hyderabad Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally. Our mission is to bring health in people’s hands by making self-care as simple as it should be. For half a billion consumers worldwide – and counting. At the core of this mission is our 100 loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world’s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan. B Corp certified in multiple markets, we are active players in the journey towards healthier people and planet. Find out more about our mission at www.opella.com. About the Role: We are looking for an experienced GxP Digital Quality professional (10-12 years) to join our Hyderabad, India team as Project Support — Digital Quality. As the global owner for Digital Quality standards, you will bring both strategic vision and operational excellence to our quality systems, ensuring compliance with global regulatory requirements and Opella's internal procedures. You will act as a Challenger — driving continuous improvement, simplifying complex processes, and partnering across functions to ensure every digital solution — from legacy systems to emerging platforms — is compliant, validated, and audit-ready. This role is for someone who owns the outcome, not just the task, and who thrives in a fast-paced, cross-functional environment where quality is everyone's responsibility. What You Will Do 1. 📋 Global Quality Policy & Documentation Governance Own it end-to-end: Act as the global owner for GxP-relevant Digital Quality Policies, Standards, SOPs, and Work Instructions — and make them work in practice, not just on paper. Manage the lifecycle: Ensure controlled document management across critical areas including CSV/CSA, Data Integrity (ALCOA+), Cloud/SaaS governance, and Electronic Records/Signatures. Keep it current: Maintain and evolve policies for Periodic Reviews and system lifecycle management, ensuring alignment with corporate and regulatory requirements. 2. ✅ Validation Expertise & Risk Management Lead planning and execution of validation and CSV activities for projects and operations, ensuring fit-for-purpose documentation — executed at pace, without waiting for perfection. Provide quality oversight and technical leadership for Computer System Validation (CSV), including management and approval of quality notifications. Collaborate with project teams, engineering, IT, and operations to support system design, testing, release, and handover. Apply risk-based approaches to validation decisions, documenting rationale clearly for all stakeholders.

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