Regulatory Information Lead

We are seeking a highly skilled Global Regulatory Operations Director to join our team at GlaxoSmithKline. In this role, you will be responsible for driving and project managing Regulatory Information risks and issues from design to execution.The successful candidate will have extensive experience in global regulatory operations and a strong understanding of...

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...

About the RoleThis is an exciting opportunity to work as a Global Regulatory Lead, driving matrix team engagement and taking ownership of life cycle maintenance, including discontinuation of Marketing Authorizations (MAs). You will lead communication with regulatory agencies, specifically be the main point of contact with the European Medicines Agency and...

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...

About the JobAs a Regulatory Systems Owner Manager, you will be responsible for overseeing the strategic management and continuous improvement of our User Access Management (UAM) application and X-Vault platform. This role ensures that UAM and X-Vault are effectively supporting global regulatory operations, compliance, and business objectives.Main...

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...

About the Role">">The Regulatory Specialist will support operational activities related to marketing authorizations across assigned markets and submission types in European Partnership Markets.">This role will provide the opportunity to lead key activities to progress your career, including supporting country leads with activities related to MA...

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...

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)...

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...

At GSK, we're constantly developing new products and improving our established medicines to improve the quality of human life by enabling people to do more, feel better and live longer. Ensuring all changes for Finished Product and Drug Substance are properly registered and up to date is essential, and that's where our CMC Delivery team's experience and...

Social network you want to login/join with:col-narrow-leftClient:Location:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:b3a17ba229a2Job Views:5Posted:15.03.2025Expiry Date:29.04.2025Job Description:We are now looking for a SENIOR REGULATORY SPECIALIST ( CTA/ IND) to join our Polish Hub.Key Responsibilities:Coordination,...

We are looking for an experienced Information Security Program Manager to join our team at Revalize, Inc. The ideal candidate will have a strong background in managing compliance programs and a proven track record of implementing effective risk mitigation strategies.Our company provides sector-specific software solutions that help manufacturers optimize...

At GlaxoSmithKline, we are looking for a skilled Data Quality Manager RIM to join our team. In this role, you will be responsible for ensuring the quality and consistency of our Regulatory Information Management (RIM) systems.The successful candidate will have extensive experience in regulatory affairs and a strong understanding of global regulatory...

Vaccine Product ManagementThis is an exciting opportunity to join our Vaccine team as a Senior Regulatory Manager, where you will play a critical role in ensuring the timely and high-quality delivery of CMC Variation dossiers. You will lead a team of direct reports, providing guidance and support to ensure seamless execution of projects.About UsWe are a...

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...

GSK is a global biopharma company dedicated to advancing science and technology to address significant healthcare challenges. We are seeking a Global Compliance Operations Lead to develop and implement effective reporting strategies that ensure compliance with global regulatory requirements.The role requires strong leadership and management skills to lead a...

Revalize, Inc. is seeking an experienced ISO 27001 Compliance Lead to join our team. The ideal candidate will have a strong background in managing compliance programs and a proven track record of implementing effective risk mitigation strategies.We provide sector-specific software solutions that help manufacturers optimize revenue operations, serving over...

We are looking for a highly skilled Medical Device Development Lead to oversee the development of our medical devices. In this role, you will be responsible for ensuring the quality and safety of our devices.Key Responsibilities:Participate in R&D projects for new medical device development and maintenance of released productsResponsible for QA aspects in...

Our company, Revalize, Inc., provides software solutions that drive revenue operations for manufacturers.We have a diverse customer base of over 10,000 companies across the globe.The Risk Management Specialist will be responsible for overseeing and maintaining ISO 27001:2022 and SOC 2 compliance across multiple brands and products.This role involves ensuring...