Quality & Regulatory Affairs (QARA) Associate - Karnataka - Cureous

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

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 Interpret data analyze results using statistical techniques provide summary reports Develop implement databases data collection systems etc. · ...

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

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 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. · ...

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 es un socio de los innovadores farmacéuticos, dispositivos médicos y productos para el cuidado del consumidor más grandes del mundo. · ...

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. · ...

In this role you will be responsible for publishing and performing technical validation of eCTD for US submissions. Performing final technical quality review. Dispatching submission to the relevant authority (eCTD/CTD/NeeS/Paper) or affiliate so that affiliate can dispatch to aut ...

+Ready to shape the future of work · At Genpact, · a transformation leader - Work at the cutting edge of AI, · automation, · and digital innovation.Come join the tech shapers and growth makers at Genpact, ...

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

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

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. · ...

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

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 ...

+End-to-end request governance for raw material data management involves timely initiation, adherence to turnaround time standards, handling supplier communication effectively, · and maintaining the Global Request Tracker. · On-time initiation within 24 hours of request receipt · ...

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. · ...