Sr. Regulatory Affairs Specialist - Hyderabad

We are seeking a Regulatory Affairs Specialist to assist Compliance and Regulatory Affairs department management in executing day-to-day tasks associated with managing, maintaining and continually improving Imaging Endpoints' regulatory systems to meet regulatory requirements. · ...

We are seeking a dedicated Regulatory Affairs Specialist - Pharma to join our team in Hyderabad. This is a full-time position designed for candidates with 1 to 3 years of experience. · Proficient in FDA regulatory submissions. · Skilled in risk management processes. · Adept at re ...

We are seeking a Regulatory Specialist to support pharmaceutical clients worldwide. · ...

We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, · disability status and genetics. Our aim is to reach over 1.5 Bn+ patients across the world by 2030. · ...

We are seeking a Regulatory Affairs Specialist to assist Compliance and Regulatory Affairs department management in executing day-to-day tasks associated with managing, maintaining and continually improving Imaging Endpoints' regulatory systems to meet regulatory requirements.The ...

This position is responsible for submissions to Health Canada for new products. · Prepare and compile regulatory submissions. · Ensure implementation of new regulatory requirements. · ...

We are seeking a Regulatory Affairs Specialist to join our team in Hyderabad. · The successful candidate will be responsible for authoring and reviewing regulatory documents, coordinating with internal stakeholders and external partners, and ensuring compliance with relevant guid ...

We are seeking a Regulatory Affairs Specialist to join our team at Orbicular Pharmaceutical Technologies Pvt Ltd. · ...

You'll lead with purpose breaking down barriers to innovation in a more connected compassionate world. · Regulatory procedures and changes. · ...

We are looking for a Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for marketing authorization applications (MAA's), regulatory support for tenders, and maintaining regulatory systems. · ...

The role requires project management and communication capacity, as well as organization skills, in alignment with Sanofi's Play to Win strategy. Project Specialists oversee and documents the creation and approval of events within their areas of responsibility within the 1CRM por ...

Supporting Design and Development Control activities with regulatory requirements. · Set up new process for entering new data - Regulatory Information Management SystemProcess SME to ensure appropriate coordination and advise on consistent interpretation of required data attribut ...

We push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. · ...

Project Specialists oversee and document the creation and approval of events within their areas of responsibility within the 1CRM portal. · ...

Project Specialists oversee and document the creation and approval of events within their areas of responsibility within the CRM portal. · ...

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. · ...

This position leads with purpose, breaking down barriers to innovation in a more connected, compassionate world. · ...

The company Medifodil Smart Pharma Solutions is expanding its Regulatory Affairs team and seeking an experienced Regulatory Affairs Specialist with 4-6 years hands-on experience. · Bachelor's or Master's degree in Pharmacy Life Sciences or a related discipline. · ...

We are looking for a Regulatory Affairs Specialist to oversee the preparation and submission of regulatory dossiers, ensuring compliance and timely approvals. · ...

Dr Reddy's Laboratories Ltd is a leading multinational pharmaceutical company based across global locations accelerating access to affordable and innovative medicines because Good Health Can't Wait. · Marketing authorization application (MAA's) - Authoring review and compilation ...