senior legal advisor - regulatory affairs - bangalore - beBeeSatellite

We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate – Authoring to join our LS Practice team. · Preparing high-quality documentation required for regulatory submissions of drugs, biologics, medical devices, · or combination products. ...

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. · 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 ...

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

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

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 ...

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

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

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 ...

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. · ...

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 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, ...

We have immediate openings for Manager – Regulatory Affairs one of our Reputed Client for Hosur location. · Preparation & Review of drug master file/ Common Technical Document of various Drug substances. · Preparation and submission of Technical Packages/ Product Dossiers. · Hand ...