Senior Associate, Content Production–Label Updates - Hyderabad

The Sr. Associate, Content Production – Label Updates is responsible for coordinating and managing activities related to Label Update development (LUD) across Amgen brands and devices. · ...

The Senior Associate, · Content Production Label Updates is responsible for coordinating and managing activities related to Label Update development (LUD) across Amgen brands and devices.Oversee artwork and content updates for IFUs and Promotional Content Labelling (PCL), ensurin ...

Summary · The role of Manager Scientific Writing involves updating / creating and reviewing scientifically / medically accurate content for commercial and medico-marketing assets such as newsletters, RTEs, civics, social media posts, websites, digital and print brochures, banners ...

Safran Electrical & Power es un líder mundial en sistemas eléctricos aéronauticos. · Crea pedidos de producción según los planes establecidos. · ...

A Labeling Technology Support Engineer plays a crucial role in ensuring the smooth operation and effectiveness of labeling systems within an organization. · ...

We are looking for a skilled Data Labeling Specialist with 3-10 years of experience to join our team in Bangalore. · ...

Support the Registrations and Dependent Objects (D0s) function, executing accurate and timely SAP master data setups for GCC lead registration required markets. · ...

Handling of pre and post approval regulatory activities of US/EU/CA submissions. Compilation and Submission of Annual reports and Supplements. · ...

+digitalized label content dlc convert traditional label information and artwork into structured digital formats collaborate with cross-functional teams including regulatory affairs to gather necessary product information and specifications validate digital label content for accu ...

The Clinical Label Expert is responsible for executing label design and reviewing related tasks in alignment with label strategy defined by the Label Lead. · This role ensures timely and accurate documentation, communication, and status reporting to support the successful deliver ...

Review of medical cases for Company and Literature and Regulatory. · ...

Design high-quality labels and graphic materials for print and digital media in line with brand guidelines. · ...

We are seeking a skilled Research Analyst-I with a strong focus on Regulatory Affairs (Authorities/Bodies) to provide detailed product profiles, regulatory intelligence, and comprehensive data analysis. · ...

A medical reviewer is responsible for reviewing medical cases and literature to ensure accuracy and compliance with regulatory requirements. They will also assess the seriousness of adverse events and code them using MedDRA. · ...

Medical writer will be responsible for medical writing tasks including aggregate reports Periodic Safety Update Reports (PSURs), Periodic Adverse Drug Experience Reports (PADERs), RMPs. · ...

+To perform Secondary research in order to provide the detailed information or the complete profile of the product. · Capturing data on companies developing drugs, devices, their descriptions, clinical trial information from press releases, · Compile and analyze data using modern ...

The Label Expert is responsible for executing label design and reviewing related tasks in alignment with label strategy defined by the Label Lead and the established processes. This role ensures timely and accurate documentation, communication, and status reporting to support the ...

The Store Executive is responsible for managing store operations including compliance & safety procedures. · ...

The Portfolio Analyst will undertake research and analysis to identify new product opportunities in Emerging Markets. · ...

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 ...