14 of 14 Permanent GxP Jobs in London

levels. Results-driven with a focus on innovation and continuous improvement. Proficiency in business intelligence and analytics tools (e.g., Tableau, Power BI). Knowledge of regulatory frameworks such as GxP, GDPR, SOX, or other compliance standards. Expertise in enterprise architecture, system integration, and process optimization. Deep understanding of financial management, supply chain, and other core ERP-supported business processes. Proficiency More ❯

Veeva Clinical Vault as an end user, business, or system administrator Ability to effectively interface with CROs and software vendor Previous experience working in clinical trials, with emphasis on GxP and compliance Has a sound working knowledge of clinical operations, clinical processes, Trial Master File regulations medical terminology, global CROs and vendor management Excellent interpersonal and communication skills, both written More ❯

Veeva Clinical Vault as an end user, business, or system administrator Ability to effectively interface with CROs and software vendor Previous experience working in clinical trials, with emphasis on GxP and compliance Has a sound working knowledge of clinical operations, clinical processes, Trial Master File regulations medical terminology, global CROs and vendor management Excellent interpersonal and communication skills, both written More ❯

management experience relevant to Haleon's scale and complexity, reflected in their scope of control Responsible for the management of Enterprise risk related to Cyber Security, Regulation, Compliance (SOX, GxP etc), Financial Reporting, Operational Stability (global business processes), Strategic Execution and Cost Management. Key Roles & Responsibilities: Accountable for defining, shaping and executing Haleons Digital strategy in support of its Sustainability More ❯

senior leadership roles aligning clinical system operations with business goals and driving innovation. Vast leadership experience in people management and large matrixed environments. Experience and vast working knowledge of GxP, CSV, data security, and IT infrastructure. Experience in leading organizational change initiatives, including the adoption of new technologies, process improvements, and system upgrades. Experience in and strong grasp of emerging More ❯

Scrum Master (CSM), SAFe Agilist, or equivalent Agile certification Agile delivery frameworks and tools (Scrum, Kanban, SAFe; Jira, Confluence, Azure DevOps) Security, privacy, and compliance in regulated environments (e.g., GxP, GDPR, ISO 27001) Application If you are interested in the role, please register your details, including a copy of your CV. Please note, while we try to respond to every More ❯

solutions. The ideal candidate will have strong technical skills, as the point person accountable for designing and approving solutions, while ensuring compliance to validation activities in a heavily regulated GxP environment. A key function of this role is the ability to partner successfully with 3rd party vendors, system integrators, SaaS vendors and internal team leads to ensure appropriate integration of More ❯

to work from home or in the office, so you can thrive in your ideal environment. Tired of working with old technology? Looking for an opportunity to change how GxP documents, quality processes, and regulatory compliance are managed in Life Sciences? Veeva's Vault Quality suite is the industry's only complete quality solution for managing quality processes with regulated More ❯

5+ years of customer-facing technical consulting experience Proven track record meeting with management and executives as the subject matter expert Experience with the Life Science Industry/with GxP and software validation regulations Experience leading and mentoring team members Ability to travel up to 20% Nice to Have Experience with Clinical, Regulatory, Quality, or Safety business processes Experience with More ❯

Clinical, pharmacological, and therapeutic knowledge of at least one disease area. Good understanding of clinical study design principles and basic familiarity working with clinical data in a clinical trial (GxP) setting. Strong knowledge and understanding of (multivariate implementations of) statistical methods such as time to event analysis, machine learning, meta-analysis, mixed effect modeling, longitudinal modeling, Bayesian methods, variable selection More ❯

Clinical, pharmacological, and therapeutic knowledge of at least one disease area. Good understanding of clinical study design principles and basic familiarity working with clinical data in a clinical trial (GxP) setting. Strong knowledge and understanding of (multivariate implementations of) statistical methods such as time to event analysis, machine learning, meta-analysis, mixed effect modeling, longitudinal modeling, Bayesian methods, variable selection More ❯

working with open-source bioinformatics tools and APIs Comfortable building end-to-end ML pipelines in cloud environments Familiarity with regulatory considerations in clinical or research settings (e.g., HIPAA, GxP More ❯

align with Orchard's strategic goals. The role focuses on process improvement, digital transformation, and cross-functional collaboration, ensuring seamless integration of ERP and patient orchestration platforms within a GxP-regulated environment. Key Responsibilities Business Process Optimization: Analyze, design, and improve SCM business processes across logistics, distribution, manufacturing, and warehousing. Lead process improvement projects, ensuring alignment with operational goals. Define … knowledge of SCM ERP modules (procurement, logistics, manufacturing, warehousing). Experience with patient orchestration platforms for Cell and Gene Therapy. Proficient in business process mapping, Lean Six Sigma, and GxP compliance. Familiar with IT and quality change control processes. Skills & Competencies: Certified Business Analysis Professional (CBAP) or equivalent preferred. Strong leadership, problem-solving, and project management skills. Excellent communication, organizational More ❯

General MasterControl administrative tasks are completed contemporaneously e.g. users are provided with access when applicable, documents are reviewed and approved in a timely manner to facilitate the progression of GxP activities All users are appropriately trained and supported when using the MasterControl Software. Documentation maintained outside of the MasterControl system is maintained in an easily retrievable state Any records overdue … limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions are closed timely and in a RFT state Job Background Minimum of 3 years experience working in a GxP environment IT literate, experience managing and operating an electronic QMS English language required Why us More ❯