Associate / Senior Associate – Regulatory Affairs (Drug Listing) - 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 ...

· Job Description: · Job Summary · The Regulatory Affairs Manager is responsible for ensuring that products are in compliance with all applicable regulations and laws. This includes developing regulatory strategies, preparing regulatory submissions. The Manager also provides gui ...

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 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 ...

Note- Candidates who can join immediately can apply · Job Description -Regulatory Affairs- Intern · Overview · We are seeking a highly motivated and experienced person to join our team · Responsibilities:Participate in the development of regulatory submission and approval strat ...

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 ...

Works effectively within a team environment · Works within broad project guidelines as directed by the Project Lead or Technical SME · Demonstrates the ability to prioritize work to achieve specified project outcomes with the guidance of the project Technical SME · Seeks feedback ...

Job Description:The Job Holder provides support to GRA Labelling staff, Regulatory Matrix Teams and Local Operating Companies to ensure the timely update, management and communication of quality regional/country Product Information (PI)/labelling and supporting documentation. The ...

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). · ...

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 ...

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. · ...

Project Objective: · To enhance efficiency, accessibility, and traceability of regulatory documentation by using the compliance tracking tool; Ricago and IT tools to support timely submissions of documentation to government authorities for sale permissions under Seed Licenses and ...

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

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 ...

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

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 ...

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, ...

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