Regulatory Affairs Specialist - Bangalore Division - Halma plc

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

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 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 ...

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. · ...

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

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 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. · ...

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. · ...

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

Main Job Tasks and Responsibilities: · Coordinate and prepare document packages for regulatory submissions (domestic and international) · Facilitate corrective actions for internal audits · Assist during governmental inspections and support related documentation · Coordinate acti ...

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. · ...

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 ...

Software As Medical devices SME job role with experience of 6 to 10 years and bachelor's degree in relevant field. · ...

Job summary · Radiometer is a company that develops medical devices and diagnostic tools. The Regulatory Affairs Specialist will be responsible for coordinating regulatory activities and providing regulatory input related to products including blood gas analyzers, immunoassay ana ...

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). ...

Software As Medical devices SME with experience in regulated industry and knowledge of FDA Quality System Regulations. · ...

In this role you will have the opportunity to drive regulatory strategy and provide guidance throughout the product system lifecycle including hardware software consumables and accessories in collaboration with a cross functional project team. · ...