Regulatory Affairs Specialist - Bengaluru

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. · ...

The Regulatory Affairs senior specialist will be responsible for planning, preparing and managing regulatory submissions and compliance activities for medical devices under CDSCO (India). The role involves working cross-functionally with design quality clinical and manufacturing ...

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

We are looking for a highly skilled and experienced Regulatory Affairs Specialist / Junior Executive to join our team at a reputed Pharma Company. · ...

Job Overview · UsefulBI is a leading AI-driven data solutions provider specializing in data engineering, cloud transformations, and AI-powered analytics for Fortune 500 companies. · The Regulatory Affairs Specialist will provide strategic and operational expertise in global and r ...

We offer you a flexible and dynamic environment and the space to stretch beyond your comfort zone to grow both personally and professionally. · ...

As Siemens Healthineers values those who dedicate their energy and passion to the cause of healthcare, our company's name is dedicated to our employees. · ...

About Halma: · Halma is a global group of life-saving technology companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US. · Our diverse group of nearly ...

At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast,and easy patient diagnoses. · ...

Job Title-Regulatory Affairs Specialist - Nutrition · Location-Unilever R&D Bangalore · About Unilever · With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and imp ...

Job Title-Regulatory Affairs Specialist - Nutrition · Location-Unilever R&D Bangalore · About Unilever · With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and imp ...

Job Title-Regulatory Affairs Specialist - Nutrition · Location-Unilever R&D Bangalore · ABOUT UNILEVER · With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and imp ...

We are an FTSE 100 company with headquarters in the UK and operations in 23 countries. · Nearly · 50 global companies specialise in market leading technologies that push the boundaries of science and technology. · ...

We are seeking a highly skilled Regulatory and Quality Systems Specialist to join our team in Bengaluru. As a key member of our organization, you will be responsible for ensuring compliance with industry specifications, standards, regulations and laws. · ...

Job Role - Software As Medical devices SME · Location- Pune/Bangalore · Experience - 6 to 10 Years · Bachelor's degree in relevant field (or equivalent experience) · 6 - 8 years working in a regulated industry (FDA and Software as a Medical Device preferred). · Strong knowledge o ...

Hiring for a Regulatory Affairs Specialist in Bengaluru. The job involves developing and implementing regional regulatory strategies for biosimilar product registrations. · ...

+Drafts and compiles technical files for international and domestic filings/registrations. · +Supports the APAC regulatory team managing international and domestic filings/registrations. · ...

A Junior Executive/Associate RA with experience in regulatory documentation and activities ,in-depth knowledge about the IVD standards to work in an ISO 13485:2016 certified Molecular diagnostic company. Experience in CDSCO, CE-IVD/IVDR, is preferred (FDA is an added advantage). ...

This Regulatory Affairs Specialist role supports APAC regulatory team managing international filings/registrations drafting technical files tender requests submission audit finding responses communicates with headquarter regulatory team on local regulation changes impact assessme ...

We are seeking a Regulatory Affairs Subject Matter Expert (SME) with 5–8 years of experience in the pharmaceutical or life sciences industry. · We help businesses turn complex data into actionable insights through our innovative products and services. · ...

As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. · ...