YASH Technologies is a leading technology integrator specializing in helping clients reimagine operating models, enhance competitiveness, optimize costs, foster exceptional stakeholder experiences, and drive business transformation. At YASH, we’re a cluster of the brightest stars working
Organization: Novo Nordisk Global Business Services (GBS) Shape the security foundation of a global SAP landscape that supports life-saving medicines reaching millions of patients worldwide. Your new role As SAP Security Architect, you will be a
Summary of Position: We are seeking a Quality Assurance Engineer to provide QA oversight for Digital Health software tools and customer‑facing supporting software systems and infrastructure within a regulated environment. In this role, you will work closely
Position Summary: The QA Specialist provides independent Quality support for GLP and GCLP studies by performing document review, protocol and experiment record review, data review, and quality event oversight activities. The role focuses on ensuring data
Position Summary: The QA Specialist provides independent Quality support for GLP and GCLP studies by performing document review, protocol and experiment record review, data review, and quality event oversight activities. The role focuses on ensuring data
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Job Title: CSV Engineer Location: Bangalore Experience: 1 -7 years Industry: Pharmaceutical / Biotechnology / Lifesciences About the Role: We are looking for an experienced Computer System Validation (CSV) professional to support validation activities for GxP-regulated computerized systems. The role involves
Exp: 8 to 12 Years Location : Bangalore/ Hyderabad NP: Immediate/30 days Job Description : Validation Lead should ensure all processes, and IT systems consistently meet safety and quality standards. They manage the IQ/OQ/PQ lifecycle and perform risk
ANSR is hiring for one of its clients. About ANSR MedTech: Who We Are: ANSR MedTech Capability Center is a new global innovation hub being established in India for a Fortune 100 Fastest-Growing Company in the
Job Summary In this role, you will be responsible for handling various computer system validation activities for different cross functional programs across West Pharma. Essential Duties and Responsibilities With guidance lead and execute validation activities for GxP computerized systems in compliance
Job Summary The IT Quality & Compliance Specialist is responsible for ensuring that computerized systems supporting regulated business processes comply with applicable regulatory requirements and industry standards. This role partners closely with IT, Quality, and business stakeholders to
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Description The Future Begins Here At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet. Bengaluru, the
Lead, develop, and execute comprehensive Computer System Validation (CSV) strategies, plans, and protocols (IQ/OQ/PQ) in compliance with FDA and global regulatory requirements. Oversee validation activities for GxP-regulated computerized systems including , manufacturing equipment software, data integrity systems, and custom applications. Ensure systems meet