Staff Regulatory Affairs - Bengaluru

We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. · The successful candidate will be responsible for LS Regulatory Authoring and/or other assigned RA activities.The role will involve knowle ...

We are seeking a highly motivated and experienced person to join our team.No relevant information about salary has been found in the job description. · ...

We are seeking a Regulatory Affairs Specialist to join our global team at Fresenius Medical Care. The successful candidate will be responsible for leading global regulatory strategy and submissions across various regions. · ...

+At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products and services across the entire healthcare journey. · +Lead global regulatory ...

We are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services and care across the entire healthcare journey. · ...

We are the global leader in kidney care committed to improving lives of patients with chronic kidney disease. Our mission is to deliver high-quality innovative products services and care across entire healthcare journey. · Lead global regulatory strategy and submissions across U ...

We are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services and care across the entire healthcare journey. · SQR also manages regulatory and quality data g ...

We are looking for a highly skilled and experienced Regulatory Affairs Executive to join our team at a reputed Pharma Company. · Develop and implement regulatory strategies to ensure compliance with industry regulations. · Prepare and review regulatory documents, including clinic ...

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. · ...

This job is with Danaher and supports new product development for Beckman Coulter Life Sciences. · ...

The Regulatory Affairs Executive will compile regulatory dossiers in various formats and review critical documents from different departments. · ...

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 ...

Beckman Coulter Life Sciences mission is to empower those seeking answers to life s most important scientific and healthcare questions. · Develop complex strategies for global registration of IVD reagents and systems · Maintain regulatory documentation, declarations, certificate ...

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 are seeking a highly experienced and meticulous Manager - Regulatory Affairs to oversee and execute all regulatory activities for drug substances and products. · ...

We are seeking a highly motivated and detail-oriented Executive Regulatory Affairs to join our dynamic team. · The ideal candidate will be responsible for ensuring compliance with regulatory requirements, · developing strategies for regulatory submissions, · maintaining documenta ...

This job is about managing the DP process for sterile injectables. · Manage DP process activities for sterile injectables. · Execute and review sterilization validation procedures. · ...

This job is with Danaher. Beckman Coulter Life Sciences mission is to empower those seeking answers to life's most important scientific and healthcare questions. · Develop complex strategies for global registration of IVD reagents and systems · Maintain regulatory documentation, ...

The Regulatory Affairs Manager will be responsible for regulatory submissions to the EU Market and Query Response. They will compile and review documents required in line with relevant guidelines and coordinate with departments to prepare submissions. · Regulatory submissions to ...