Regulatory Information Management Lead

The Senior Manager, RIM & Data Office at GlaxoSmithKline is responsible for ensuring the timely execution of RIM based requests and delivery of RIM initiatives and projects. This includes overseeing operational teams and leading matrix teams across the broader Regulatory Information Management & Data Office and Global Regulatory Operations group,...

Key ResponsibilitiesAct as Global Regulatory Lead: Drive matrix team engagement for CEP portfolio assets and take ownership of lifecycle maintenance, including discontinuation of Marketing Authorizations (MAs).Lead Communication with Regulatory Agencies: Be the main point of contact with the European Medicines Agency and other European Local Health...

We are seeking a Senior Manager, RIM & Data Office at GlaxoSmithKline to lead our Regulatory Information Management efforts. In this role, you will oversee operational teams and lead matrix teams across the broader Regulatory Information Management & Data Office and Global Regulatory Operations group, globally.Your responsibilities will include partnering...

About the RoleWe are seeking a skilled and experienced Global Regulatory Operations Leader to join our team at GlaxoSmithKline (GSK). As a key member of our organization, 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 is critical in...

About the Job:We are looking for a talented CMC Regulatory Expert to support our Global Regulatory Centres in GSK. The ideal candidate will have extensive experience in regulatory affairs, pharmaceutical industry, and familiarity with CMC regulatory procedures and ICH CTD documentation.Key Requirements:Bachelor's or Master's degree in biotechnology,...

Job DescriptionWe are seeking an ambitious Regulatory Project Manager to lead the development of regulatory strategies and their execution for assigned assets, ensuring compliance with internal GSK processes and external regulatory requirements.The successful candidate will create a place where people can grow, be their best, be safe, and feel welcome,...

GSK is a global biopharma company with a special purpose – to unite science, technology, and talent to get ahead of disease together.We are committed to delivering high-quality products to patients worldwide while ensuring the highest standards of regulatory compliance and operational efficiency.About the Role:This role is a key part of our regulatory...

As a Senior Manager, RIM & Data Office at GlaxoSmithKline, you will play a critical role in ensuring the timely execution of RIM based requests and delivery of RIM initiatives and projects. You will oversee operational teams and lead matrix teams across the broader Regulatory Information Management & Data Office and Global Regulatory Operations group,...

About the RoleWe are seeking a highly skilled Senior Manager, Regulatory Operations to lead our Veeva Regulatory Vault team. As the Business System Owner (BSO), you will be responsible for overseeing the strategic management and continuous improvement of this business-critical system.As BSO, you will ensure that Reg Vault is effectively supporting global...

About UsGSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together. We are committed to positively impacting the health of billions of people and delivering stronger, more sustainable shareholder returns.We are seeking a highly skilled Senior Manager, Regulatory Operations to join our...

At GlaxoSmithKline (GSK), we are seeking a talented Senior Manager to join our team as the Business System Owner for Veeva Regulatory Vault. As a key member of our regulatory operations team, you will be responsible for overseeing the strategic management and continuous improvement of this critical business system.This role is instrumental in ensuring that...

The Senior Regulatory Specialist, Country Labelling will play a key role in ensuring that all labelling documents and related materials meet the highest standards of quality and compliance. This includes coordinating with internal stakeholders to gather necessary information and conducting thorough reviews to ensure accuracy and completeness. The role will...

Company OverviewGSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with...

About the RoleThe Senior Reporting Manager will be responsible for leading the reporting of resource management data, ensuring accurate, timely, and insightful analysis to support decision-making across GSK's R&D organization.This role will work closely with various stakeholders, including Resource Managers, PPM/DDAP and functions, to ensure the effective...

At TN Poland, we're building the world we want tomorrow, today.About the RoleThis is a challenging opportunity for an experienced Digital Transformation Lead to join our team and drive the implementation of vendor data management solutions across the organization.You will be responsible for leading the development and deployment of global templates for...

Information Security Investigations LeadTN Poland is seeking a highly skilled Information Security Investigations Lead to join our team. In this role, you will work within the firm's Insider Risk function to conduct complex and confidential investigations into incidents of data loss and intellectual property theft.You will partner with and report into the...

We are seeking a highly skilled CMC Regulatory Expert to join our team at Randstad Polska Sp. z o.o.Job Description:Manage multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers)Lead...

As a Senior Compliance Specialist, you will be responsible for managing multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers).About the Job:Lead assigned projects: define and agree...

We are looking for a Regulatory Affairs Specialist to join our team at Randstad Polska Sp. z o.o.About the Role:Manage multiple CMC variations and source transfers for Finished Products, Intermediates and Active Pharmaceutical Ingredients for pharmaceutical, biopharm and vaccines products (work with the CTD Module 3, Quality part of the dossiers)Lead...

About the RoleWe are seeking a highly skilled Regulatory Systems Business Owner to join our team at GlaxoSmithKline (GSK). As a key member of our organization, 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 requires a deep understanding...