Medical Affairs Manager - Hyderabad

Azurity Pharmaceuticals is a privately held specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. · ...

Regulatory Affairs Manager facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. · ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected compassionate world. · ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You ll lead with purpose, breaking down barriers to innovation in a more connected compassionate world. · ...

Role & responsibilities · Follow and adhere to Good manufacturing practices (GMP), Good document practices (GDP) and Data integrity (DI). · Compilation and review of drug master files as per various regulatory agencies/authorities. · Preparation, compilation and review of dossier ...

In this exciting role as a Regulatory Affairs Manager at Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. · ...

A Regulatory Affairs Manager will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. · ...

The Regulatory Affairs Manager will develop regulatory strategies for drug approval, prepare submissions to authorities, liaise with regulatory agencies, monitor compliance and ensure labeling accuracy. · Regulatory Strategy Development · Preparation and Submission of Regulatory ...

Manager – Academic and Student Affairs · (Academic Associates and Academic Advising) · 1. Academic & Course Operations · Coordinate timely and accurate course setup, including LMS integration, material uploads, and academic resource readiness. · Track grading progress and compone ...

Regulatory Affairs Manager – Devices · What you will do · Let's do this. Let's change the world. In this vital role you will support development and execution of regulatory strategies and filings for new and existing drug delivery devices and combination products, establishing su ...

Key Responsibilities · Support the implementation of automation and digital tools to streamline regulatory CMC documentation and submission workflows. · Assist in developing standardized templates and structured data formats to ensure consistent and compliant submissions. · Contr ...

Job Description: · Qualifications: · B. Pharm / M. Pharm / M.Sc · Experience: · 10–14 years · Key Responsibilities: · Prepare, compile, and submit regulatory dossiers and submission data. · Manage Test and Manufacturing License applications with state and central drug authorities ...

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated cap ...

The RA CMC Manager is responsible for execution and/or coordination of global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial produ ...

Manager – Academic and Student Affairs · (Academic Associates and Academic Advising) · 1. Academic & Course Operations · Coordinate timely and accurate course setup, including LMS integration, material uploads, and academic resource readiness. · Track grading progress and compone ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for execution of post-marketing regulatory activities for MENA ...

Regulatory Affairs Leader with global experience across US, EU, Canada & Australia. Skilled in IND, NDA, BLA, MAA, NDS, submissions, CTD/eCTD publishing, lifecycle management, GMP compliance, health authority liaison, inspections & team leadership. · ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented  · Regulatory Affairs Post-Approval Manager · to join our team. The candidate will be responsible for managing variations, life-cycle management, and compli ...

This is a full-time, on-site position based in Hyderabad for a Manager-Regulatory Affairs (Pharma Domestic) at Jaidev Pharma Placement. · ...

At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate will be responsible for managing variations, life-cycle management, and compliance ...