Senior Regulatory Affairs Consultant II - Bengaluru, Karnataka, India

We are seeking a full-time Regulatory Affairs Consultant for an on-site role located in Mumbai. This position involves direct client interaction, managing regulatory submissions, providing compliance guidance and assisting clients with meeting regulatory requirements across diver ...

A regulatory affairs consultant with around 7-10 years of experience in handling life cycle management of drug products. · ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. · ...

Around 7-10 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products. · ...

Regulatory Affairs Consultant at Parexel. · 6 years of experience in handling new registrations and renewals of Biologicals and Vaccines in various markets. · Contribute to preparation and delivery of regulatory submissions from a global perspective. · ...

We are seeking an experienced Senior QARA Consultant with strong expertise in Regulatory Affairs for Medical Devices IVD and SaMD products. · Lead and manage Regulatory Affairs activities for Medical Devices IVD and SaMD products. · Prepare review and submit regulatory dossiers i ...

We are seeking an experienced Senior QARA Consultant with strong expertise in Regulatory Affairs for Medical Devices, IVD, and SaMD products. · The ideal candidate will lead regulatory submissions, product registrations, and compliance activities while working closely with cross- ...

Syner-G seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large global pharmaceutical client in the areas of Chemistry Manufacturing and Controls ...

Syner-G seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, EMA, and global regulatory requirements. · ...

Syner-G seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, · EMA,and global regulatory requirements. · Demonstr ...

Syner-G seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, EMA, and global regulatory requirements (with a focu ...

Syner-G BioPharma Group seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, EMA, and global regulatory requireme ...

Syner-G BioPharma Group seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, EMA, and global regulatory requireme ...

Syner-G BioPharma Group seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large, global pharmaceutical Client in the areas of Chemistry, Manufacturing, and Controls (CMC), to ensure compliance with FDA, EMA, and global regulatory requireme ...

Syner-G BioPharma Group seeks a Manager/Senior Manager of Regulatory Affairs to provide regulatory consulting to a large global pharmaceutical Client in the areas of Chemistry Manufacturing and Controls CMC to ensure compliance with FDA EMA and global regulations. · ...

We are seeking an experienced Senior QARA Consultant with strong expertise in Regulatory Affairs for Medical Devices IVD and SaMD products. · ...

We are seeking a Junior Consultant to support senior case leads on high-sensitivity client engagements. · Support Senior Consultants in delivering diagnostic assessments, stakeholder interviews, investigative analysis and organisational research ...

MindFriend Pro is seeking a Junior Consultant to support senior case leads on high-sensitivity client engagements. · Support Senior Consultants in delivering diagnostic assessments and investigative analysis · ...

The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. · ...

Provide strategic legal guidance relating to business activities across India and handle governance matters. · ...