11 of 11 GxP Jobs in the North of England

testable requirements and operational evidence; contribute to threat modeling and risk assessment using leading frameworks; support risk-tiered controls across research, business, regulated and GxP-relevant use cases; document residual risk, control limitations, exceptions and approvals to enable defensible decisions; engage vendors and peers to evaluate capabilities and shape adoption ...

stability, governance, and service excellence across global Manufacturing, Supply Chain, and Quality teams. Lead vendor management for AMS partners, define Run playbooks, and ensure GxP compliance while advancing automation and efficiency initiatives within a regulated pharma context. #J-18808-Ljbffr ...

ensure business continuity. Utilise the service management tool (e.g. ServiceNow) to record, update, and manage incidents. Security, Compliance & OT Considerations Implement and maintain GxP-compliant IT infrastructure within a regulated pharmaceutical environment. Ensure CFR Part 11 and data integrity requirements are met across all IT/OT systems. Implement cybersecurity ...

enhancements and new implementations. You will be responsible for generating validation documentation and ensuring systems are maintained in a validated state, compliant with GxP and data integrity requirements.Stakeholder Collaboration: Work closely with Manufacturing Operations, Quality Assurance, and Process Science teams to gather system requirements and provide updates on technical activities.User … Emerson Syncade, POMSnet).Manufacturing Environment Experience: Experience working directly in a manufacturing environment, preferably within the pharmaceutical, biologics, animal health, or another GxP-regulated industry.Regulatory Knowledge: A working knowledge of GxP (Good Manufacturing Practices) and familiarity with computer system validation (CSV) principles.Process Control Understanding: Familiarity with industrial automation concepts, including ...

trails, electronic signatures, role-based access, segregation of duties, data integrity, master data, time synchronisation and lifecycle controls . Ensure architectural decisions support GMP, GxP, data integrity, patient safety, product quality and inspection readiness . Partner with Engineering, Automation, Manufacturing, Quality, Validation, Cybersecurity, Infrastructure, Data, Applications and senior site stakeholders. … have: Strong experience designing OT/IT architectures within pharmaceutical, life sciences, chemical, food & beverage or similarly regulated manufacturing environments . Strong understanding of GxP/GMP regulated environments and the implications these have on technology architecture. Experience with IT/OT convergence and industrial control environments . Strong understanding ...

Support the operational quality, validation, maintenance, and optimisation of site technologies and facilities (MSAT, engineering and logistics) to ensure compliance with regulatory requirements and GXP standards. Assist in the implementation and documentation of technology systems and facility processes, ensuring alignment with quality and operational goals. Collaborate with cross-functional teams … shape their development. Join us and help deliver high quality supply while growing your skills and impact. Skills Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Problem Solving, Project Management, Quality Assurance (QA), Risk Awareness, Technical Writing, Validation Processes Why GSK? Uniting science, technology ...

stakeholders (e.g., SAP Functional Leads, Data Integrity teams, Solution Architects and other Operation Managers covering different service lines) to ensure service suitability and GxP compliance. Leadership Reporting: Interactions with Senior IT and Business leadership regarding ERP performance, status of major incidents, and reporting on service improvement initiatives. Efficiency & Automation: Work … scalable model for other ERP modules. Partnering with ERP stakeholders to understand business-critical cycles and ensure IT operations support peak demand. Ensuring GxP compliance and quality practices are embedded in every SAP change and operational activity. Attending the weekly CAB and Problem Review Board to ensure ERP operational perspectives ...

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and ...

We'rebuilding a connected, end-to-end Enterprise AI engine - uniting data foundations, AI technology, process reinvention, and business-facing AI to accelerate results across the whole value chain. Success depends on being exceptional connectors ...

Location: Liverpool, UK – Onsite Duration: ~12 Months Industry: Pharmaceutical/Life Sciences Role Overview Seeking an experienced CSV Engineer to support a large-scale GxP validation, remediation, qualification, and systems improvement project. The role involves managing multiple workstreams across computerized systems. Key Responsibilities Develop CSV Plans aligned with … across the site. Implement and validate Wonderware/user management for the Pall water system. Support and validate Octoplant server activities. Install and validate GxP Manager . Review and standardize HMI naming conventions for improved traceability. Prepare and execute risk assessments, IQ/OQ/PQ protocols, test scripts, deviations ...

Compliance Group Inc. is seeking an experienced CSV Engineer in Liverpool, onsite, to support a large-scale GxP validation and remediation project. You will manage multiple workstreams across computerized systems. Key responsibilities include developing CSV plans, reviewing CSRA and PQE, and installing/qualifying audit trails, IP clocks, and Wonderware ...