Regulatory Affairs Associate I - Navi Mumbai

We are looking for a highly skilled and experienced Regulatory Affairs Associate to join our team at a reputed Pharma Company. · The ideal candidate will have a strong background in regulatory affairs and a minimum of 2 to 5 years of experience.Develop and implement regulatory st ...

We are looking for a highly skilled and experienced Regulatory Affairs Associate I to join our team. The ideal candidate will have a strong background in regulatory affairs, preferably in the pharmaceutical and life sciences industry. · Roles and Responsibility · Develop and impl ...

As a Regulatory Affairs Associate I at Teva Pharmaceuticals, you will participate in the publishing of different regulatory activities and ensure 100% quality and timeline of submissions. · Publish and dispatch major and complex routine/lifecycle management eCTD submission projec ...

We are on a mission to make good health more affordable and accessible. We work with the world's leading manufacturer of generic medicines and produce many products on the World Health Organization's Essential Medicines List. · Publish and dispatch major eCTD submission projects ...

+Job summary · We Are Teva · ++Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada. · Exposure in handling post approval submissions publishing and transmitting quality submissions to agency. · Perform document level ...

We Are Teva · We're Teva, a leading innovative biopharmaceutical company, · enabled by a world-class generics business. · The opportunity · The Associate III prepares and submits high-quality regulatory submissions to the FDA within timelines. · ...

+Job summary · Associates will work with minimal to no guidance to prepare and submit high quality regulatory submissions within company timelines. The role involves maintaining approved applications in compliance with FDA regulations, independently evaluating change controls and ...

We are Teva, · a leading innovative biopharmaceutical company, · enabled by a world-class generics business.Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in ...

Prepares regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines. · ...

· The Regulatory Affairs associate I – RA publishing will participate in the publishing of different regulatory activities.Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada. · Perform document level publishing acti ...

We Are Teva · We're Teva, a leading innovative biopharmaceutical company.Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide,We are dedicated to addressing patients' needs now and in the future. · M. Pharma degree in ...

This role involves preparing regulatory submissions such as supplements and annual reports in accordance with FDA guidelines. · Prepare annual reports under direct supervision. · Assist in supplements for FDA submissions. · ...

We Are Teva is a leading innovative biopharmaceutical company that enables a world-class generics business. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life w ...

We Are TevaWe're Teva,a leading innovative biopharmaceutical company,whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, · we're dedicated to addressing patients' needs now and in the future. · The opportunity · Unde ...

· patients' needs now and in the future. · regulatory submissions such as supplements annual reports in accordance to FDA guidelines. · ...

Teva es una empresa innovadora en el sector farmacéutico. Aquí, se busca un Regulatory Affairs Associate para participar en la publicación de actividades regulatorias. · Se requiere experiencia en publicación y despliegue de proyectos eCTD para EU, US y Canada. · ...

We're Teva, a leading innovative biopharmaceutical company. · Under direct supervision, prepare annual reports and as experience is gained assist in supplements for FDA submissions. · Maintain approved applications in compliance with FDA regulations for assigned ANDA Annual Repor ...

We're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. · ...

We're Teva a leading innovative biopharmaceutical company enabled by a world-class generics business Here you will be part of a high-performing inclusive culture that values fresh thinking collaboration You'll have the room to grow flexibility to balance life with work and the op ...

We're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. · The opportunity is to execute the operations and services applicable to the GRO Regulatory Data Analytics role in line with business goals and objecti ...

We are Teva · We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs ...