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Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
We are looking for a strong and experienced Senior Validation Lead to guide and execute the Computerized System Validation/Assurance of IT systems and projects within our Research and Development (R&D) division. This role is critical in ensuring that our IT systems comply with regulatory requirements and industry standards, thereby supporting our mission to deliver high-quality pharmaceutical products for patients.
The ideal candidate will have extensive experience in FDA 21 CFR Part 11, EU Annex 11, GVP regulations, and GAMP GxP computerized systems validation. Familiarity with the ISPE GAMP AI Guide, AI Guidance for GxP environments, and the EU AI Act will add additional value. The candidate should also possess a solid understanding of Agile development under GxP conditions, act and decide risk based and strengthen this mindset within the team.
In this role, you will guide IT Vendor Management and IT Service Delivery with your regulatory expertise, providing input, support and address IT Vendor audits. You will also guide and supervise corrective and preventive actions (CAPA) as part of the deviation management and continuous improvement process. Collaborating closely with project teams, you will ensure compliance throughout the project lifecycle. With this you are responsible for Audit and Inspection readiness, present and explain compliance documentation and processes during internal audits and external inspections.
Key Responsibilities:
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