Regulatory Affairs Associate II - Bengaluru

Regulatory Affairs Associate · Relevant years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. · To understand the regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules acros ...

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. · ...

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. · ...

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. · ...

Relevant years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. · To understand the regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions. · To provide reg ...

ZEISS in India · ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics. · ZEISS India has 3 production facilities, R&D center, Global IT servi ...

ZEISS in India · ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics. · ZEISS India has 3 production facilities, R&D center, Global IT servi ...

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 ...

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 ...

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. · ...

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. · ...

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

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

Assessment of Change Controls: · Evaluate change controls for registration impact and ensure implementation of necessary dossier changes in Europe and International Markets. · Variations Compilation: · Compile variation packages for products in the portfolio in collaboration with ...

The role of an Associate - Regulatory Affairs (RMQ) involves end-to-end request governance for raw material data management. The candidate should have technical expertise in regulatory requirements for raw materials within all categories of use. · ...

We Are Teva. We're Teva, a leading innovative biopharmaceutical company. Here, you will be part of a high-performing culture that values fresh thinking and collaboration. · Providing regulatory support for European Market RA, · Completion of designated projects and tasks supporti ...

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 ...