11 of 11 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 ❯

and transforming lives. Role Objectives: The WEP Clinical Global Third-Party and Audit Manager is responsible for the qualification, oversight, and auditing of third-party suppliers and vendors supporting GxP activities, including pharmaceutical manufacturing, distribution, and clinical operations. This includes providers across GMP, GDP, GCP, GLP, and GVP domains. The role ensures partners meet regulatory requirements and internal standards to … framework through risk-based oversight and cross-functional collaboration. The Ideal Candidate: Analytical Collaborative Adaptable Proactive What You'll Do: Own and lead global compliance monitoring programs for all GxP third parties, ensuring timely qualification, requalification, or disqualification. Design and manage a global, risk-based GxP audit program covering GMP, GDP, GCP, GLP, and GVP audits, both remote and on … on CAPA completion. Maintain and assess approved supplier and vendor lists, including criticality ratings and compliance status. Ensure all qualification and requalification activities align with EU, UK, and FDA GxP expectations and internal SOPs. Monitor ongoing third-party performance using audits, KPIs, deviations, complaints, and quality metrics. Lead risk-based internal audit programs and delegate audits to appropriately qualified personnel. More ❯

the pharmaceuticals industry. Strong experience in a Scrum Master role. Proven experience in both Agile and traditional project delivery environments. Excellent organizational, facilitation, and communication skills. Strong understanding of GxP (Good Practice) guidelines. Preferably prior experience with project management. More ❯

integration teams to ensure accurate implementation. Support ERP project delivery, including workshops, UAT, training, change management, and golive support. Collaborate with compliance and validation teams to ensure solutions meet GxP and audit requirements Required Skills & Experience Demonstrated track record in business analysis, with a strong focus on ERP systems— particularly Microsoft Dynamics 365 Finance & Operations (D365 F&O). Proven … expertise in Supply Chain and Manufacturing modules (inventory, procurement, production, demand planning). Experience in the pharmaceutical industry or a similarly regulated, GxP-compliant environment. Strong understanding of ERP best practices, master data management, and process transformation in global organizations. Skilled in gathering requirements, facilitating workshops, and producing high-quality documentation. Strong stakeholder management and communication skills across technical and More ❯

of Claims, DAM (Digital Asset Management), Modular Content, MLR review, and European regulatory requirements (e.g., ABPI, ANSM, AIFA) Understanding of life sciences compliance and computer systems validation requirements (e.g., GxP, GcP) Project management certification (e.g,. PRINCE2, PMP) Experience with product pre-sales, solution consulting, or engagement management Fluency in Italian, French, or German SaaS/Cloud experience Veeva's 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 ❯

supply, demand, PPDS, inventory) Troubleshoot daily planning issues and drive root-cause resolution Deliver RICEFW objects and functional documentation Support testing, training, and go-live activities Ensure compliance with GxP and SOX requirements Required Experience: 10+ years in SAP supply chain planning, including S/4 ePPDS and IBP Deep knowledge of IBP modules: Response & Supply, Inventory, S&OP, Control 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 ❯

controls, and Computer System Validation (CSV). Excellent communication, documentation, and stakeholder engagement skills. Desirable Skills: Experience with SAP S/4HANA implementations or finance transformation initiatives. Familiarity with GxP and data privacy regulations such as GDPR. Relevant certifications (e.g. CISA, CISM, SAP FICO). Understanding of UK and international financial reporting standards. If this role is of interest please More ❯

controls, and Computer System Validation (CSV). Excellent communication, documentation, and stakeholder engagement skills. Desirable Skills: Experience with SAP S/4HANA implementations or finance transformation initiatives. Familiarity with GxP and data privacy regulations such as GDPR. Relevant certifications (e.g. CISA, CISM, SAP FICO). Understanding of UK and international financial reporting standards. If this role is of interest please More ❯

fast-growing, regulated environment with plenty of moving parts. Your mission: keep things running smoothly and the regulators smiling. What you’ll be doing - Supporting IT system implementations and GxP upgrades - Preparing evidence for audits (FDA, MHRA, etc.) - Tracking CAPAs and business-driven compliance requests - Contributing to compliance automation tool implementation - Working across IT infrastructure and GxP applications - Helping the More ❯