Regulatory Affairs Expert

This exciting opportunity is for a highly skilled and experienced professional to join our Regulatory Affairs department as a Regulatory Affairs Director - New Registrations. You will be responsible for leading our CMC RA team in delivering regulatory excellence, ensuring timely preparation and submission of high-quality CMC documentation.You will also...

We are seeking a highly skilled Regulatory Affairs and Quality Manager to ensure the compliance of our medical devices with regulatory requirements. In this role, you will be responsible for leading risk management, usability, design verification & validation activities.Key Responsibilities:Lead risk management, usability, design verification & validation...

Job Title: Regulatory Affairs and Quality EngineerJoin our team as a Regulatory Affairs and Quality Engineer and contribute to the development and maintenance of our medical devices. You will be responsible for ensuring compliance with regulatory requirements and industry standards.Responsibilities:Regulatory Compliance: Ensure our medical devices comply...

The Regulatory Manager will be responsible for managing people aspects of a team of direct reports to create and sustain an efficient, qualified and motivating working environment.You will efficiently plan and ensure timely delivery and high quality of Pharma, Biopharm and Vaccines CMC projects. You will identify risks to quality and/or timely completion of...

Role Summary:As a Senior Specialist, Reporting and Analytics, you will be responsible for the development, implementation, and maintenance of reporting services that support regulatory operations on a global scale.This role requires collaboration with cross-functional teams, including Regulatory Affairs, IT, Quality, and other stakeholders, to drive...

About the Role:As a Senior Specialist, Reporting and Analytics, you will be responsible for developing, implementing, and maintaining reporting services that support regulatory operations on a global scale.This role ensures the delivery of high-quality, compliant, and timely regulatory reports that meet business needs and regulatory requirements across...

We are seeking a highly skilled Regulatory Information Lead to join our team at GlaxoSmithKline. In this role, you will be responsible for leading initiatives and projects to support evolving internal and external regulatory requirements impacting RIM processes.The successful candidate will have extensive experience in regulatory affairs and a strong...

At GlaxoSmithKline, we are committed to excellence in regulatory operations reporting. As a Senior Regulatory Reporting Specialist, you will be responsible for developing and implementing comprehensive reporting strategies that align with our global regulatory goals and objectives.The role ensures the delivery of high-quality, compliant, and timely...

Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people.Senior Product Expert- RegulatoryAbout the roleProduct Expert- Regulatory is accountable for all aspects of the Regulatory technology ecosystem relating to Regulatory vault, Publishing, including but...

In this role, you will be part of Allegro's Risk & Compliance team, which plays a vital role in ensuring the company's operations comply with applicable laws in Poland and Europe.The key responsibilities include:Collaboration with Allegro Group teams to ensure compliance with regulatory requirements.Implementation of legal acts, including impact analysis,...

About UsAt Allegro, we are committed to creating a safe and secure online environment for our users. As a Regulatory Compliance Expert, you will play a critical role in ensuring that our platform remains compliant with regulatory requirements and industry best practices.Your Key ResponsibilitiesDevelop and implement effective AML/KYC strategies and...

Job Description:The Global Regulatory Operations Reporting Specialist at GlaxoSmithKline (GSK) is responsible for development, implementation, and maintenance of reporting services that support regulatory operations on a global scale.This role requires collaboration with cross-functional teams, including Regulatory Affairs, IT, Quality, and other...

Dynamic Career OpportunityJoin Allegro e-Xperience 2025 as a Junior Content Compliance Specialist and embark on an exciting journey that fosters personal growth and development. This role is ideal for someone who thrives in collaborative environments and enjoys navigating complex regulations.About the PositionAs a key member of our team, you will work...

Social network you want to login/join with:Client:Location:Job Category:OtherEU work permit required:YesJob Reference:1b8faa66fc70Job Views:3Posted:18.03.2025Expiry Date:02.05.2025Job Description:The Regulatory Specialist supports operational activities related to the maintenance of marketing authorisations (MAs) across assigned markets and/or submission...

The role of Senior Regulatory Project Lead is crucial in ensuring that GSK's pharmaceutical products meet the highest regulatory standards. As a key member of our CMC RA team, you will be responsible for assessing, managing, and driving the CMC strategy for new chemical entities, product expansions, and CTA submissions.You will work closely with...

Senior Regulatory Affairs ExpertDo you have a proven track record of navigating complex regulations? Are you passionate about driving change through collaboration? As a Senior Regulatory Affairs Expert within Allegro e-Xperience 2025, you will lead the way in shaping our regulatory landscape.About the RoleResponsibilities include:Leading cross-functional...

Client:Location:Job Category: OtherEU work permit required: YesJob Reference: 6f70661ca09dJob Views: 6Posted: 16.03.2025Job Description:What we are doing?Global Regulatory Centres (GRC) in GSK are regulatory affairs functions which bring together the operation and execution aspects for key regulatory deliverables such as new chemical entity and product...

About the Position:This EMEA Quality Support Specialist position is part of our Business Quality organization, responsible for providing quality support and regulatory compliance across the EMEA region. The successful candidate will work closely with local teams and stakeholders to ensure compliance with regional regulations.Main Responsibilities:Support the...

At WS Audiology, we are committed to making wonderful sound a part of everyone's life. To support this mission, we are looking for a Senior Business Quality Specialist to identify and oversee regulatory requirements across the EMEA region.In this role, you will be a vital part of the Business Quality organization, working closely with peers across EMEA and...

Social network you want to login/join with:Client:Location:Job Category:OtherEU work permit required:YesJob Reference:ea5eca9918baJob Views:3Posted:17.03.2025Expiry Date:01.05.2025Job Description:We are looking for an ambitious Regulatory Project Manager to ensure the development of regulatory strategy(ies) and their execution for assigned asset(s)...