Regulatory Affairs Associate II - Bengaluru

The role involves collating data from primary/secondary sources or stakeholders and maintaining databases and data systems. · Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems · Interpret data, analyse results using statistic ...

Collate data from primary/secondary data sources or stakeholders · and maintain databases and data systems. · ...

Collate data from primary/secondary data sources or stakeholders and maintain databases and data systems Interpret data analyze results using statistical techniques provide summary reports Develop implement databases data collection systems etc. · ...

This job is about managing the DP process for sterile injectables. · Manage DP process activities for sterile injectables. · Execute and review sterilization validation procedures. · ...

We are looking for a passionate and detail-oriented Regulatory Affairs Specialist (Fresher) to join our life sciences and healthcare compliance team. · ...

We are seeking a highly motivated and detail-oriented Regulatory Specialist to play a critical role in ensuring our medical device development processes meet the highest standards of quality and regulatory compliance. · ...

Job Title: Regulatory Affairs Associate – ICSR & Aggregate Reporting · Location: Remote / Bangalore · Experience: 3–5 years · Employment Type: Full-time · About the Role · We are seeking a detail-oriented and experienced · Regulatory Affairs Associate · with hands-on expertise in ...

Perform required data clean-up as per the defined process in the Regulatory Information Management System (RIMS). Support business users by reviewing the data entered into the RIMS application and providing updates to users. Complete assigned user requests on a daily basis as per ...

ClinChoice is a partner to pharmaceutical innovators in the world. · Perform required data clean-up as per the defined process in RIMS. · ...

The job is for a Regulatory Affairs Associate at ClinChoice in Bengaluru, India. The role involves data clean-up and submission intake requests using the Regulatory Information Management System (RIMS). Candidates should have experience with RIMS software and document management ...

· Job Title: Associate – Regulatory Affairs (RegPoint) · Employment Type: Full-time (Permanent) · Location: Bengaluru, India · Work Type: Office-based · Experience: 0–1 year · About ClinChoice · ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer ...

ClinChoice es un socio clave para los principales innovadores farmacéuticos, dispositivos médicos y productos de cuidado del mundo. · Se requiere experiencia en RIMS regulatory data management. · Se busca candidato con B.Pharm o M.Pharm. · ...

The Regulatory Affairs Associate III will lead regulatory affairs activities independently for assigned projects ensuring compliance with global regulatory requirements. · ...

Ready to shape the future of work · At Genpact, we don't just adapt to change-we drive it. AI and digital innovation are redefining industries, and we're leading the charge. Genpact's AI Gigafactory, our industry-first accelerator, is an example of how we're scaling advanced tech ...

Ready to shape the future of work · At Genpact, we don't just adapt to change-we drive it. AI and digital innovation are redefining industries, and we're leading the charge. Genpact's AI Gigafactory, our industry-first accelerator, is an example of how we're scaling advanced tech ...

This is a Regulatory Affairs Associate II role that involves providing regulatory support for European Market RA. · ...

This role involves end-to-end request governance for raw material data management. · ...

This is a Regulatory Affairs Associate III position at Teva Pharmaceuticals. The job involves leading and executing regulatory affairs activities independently for assigned projects. Key responsibilities include post-approval change impact assessment, classification of change cat ...

This role involves end-to-end request governance for raw material data management. · Initiate requests within 24 hours of receipt. · Adhere to turnaround times for all requests. · ...

Responsible for independently leading and executing all the Regulatory Affairs activities. · ...