Associate - Ra Publishing

**Job Summary**: **Key Responsibilities**: - Prepare, review, and compile regulatory submissions in eCTD/aCTD formats for various markets including the US, UK, EU, and ROW. - Ensure submissions are compliant with the regulatory guidelines and are ready for on-time dispatch. - Manage and track the status of submissions and respond to regulatory agencies'...

**Summary**: Provide regulatory CMC operational, submission and compliance support to department in accordance to defined requirements to guarantee timely preparation of high-quality CMC regulatory submissions and associated compliance information throughout the life cycle. **About the Role**: **Major accountabilities**: - Perform compliance and...

Education: Bachelors Degree in Life Sciences or related fieldMarkets: US/UK/EU/ROW Job Summary:We are seeking a detail-oriented and proactive Associate - Regulatory Affairs (RA) Publishing with 1-3 years of experience in regulatory submissions across global markets including the US, UK, EU, and ROW (Rest of World). The ideal candidate will have a background...

Summary -Responsible for regulatory activities specifically related to chemistry manufacturing and control CMC Activities such as the preparation publication of REG CMC documentation for submissions to Health Authorities In addition interact with HA s on REG CMC questions to support new product or post marketed launches Major accountabilities ...

Job Description Summary -Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC).Activities such as the preparation & publication of REG CMC documentation for submissions to Health Authorities.In addition interact with HA's on REG CMC questions to support new product or post marketed launches.Job...

**Summary**: Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs), and provide publishing consultancy to the clinical teams and other line functions. **About the Role**: Key Responsibilities - In...

Job DescriptionMajor accountabilities:- Formulate and lead global CMC regulatory strategy with a focus on innovation, maximizing the business benefit balanced with regulatory compliance -Lead and implement all global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products.- Identify the required...

Job Description Hello. Were Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, were improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum through a unique combination of...

Summary The role of Service Delivery Associate Director in Hyderabad focuses on leading the strategic and operational implementation of Veeva Vault in Regulatory Affairs ensuring alignment with organizational goals and regulatory compliance This position requires extensive experience in project leadership data migration Validation and testing and...

Associate III - Business Analysis Regulatory Affairs - Life Sciences Publishing Role Summary The Associate III - Business Analyst Regulatory Affairs - Publishing plays a crucial role in supporting regulatory operations within the life sciences industry This role involves understanding stakeholder needs gathering and analyzing requirements and...