51 to 75 of 94 GxP Jobs in England

industry role Experience working with one or more R&D operational roles (clinical operations, regulatory, safety or similar discipline) either in industry or consulting GxP System Implementation and Validation experience Desired Requirements: Experience supporting implementations of cloud-based enterprise software such as Veeva Vault, Oracle, Medidata or OpenText Why Syneos ...

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/ ...

complex technical solutions in an enterprise software environmentStrong ability to communicate complex concepts to senior business and technical stakeholdersFamiliarity with Life Sciences industry regulations (GxP, validation processes)Proven ability to lead, mentor, and inspire cross-functional teamsAbility to travel up to 20% across Europe as neededNice to HaveDirect experience ...

testing across areas such as analytical, microbiology, biochemistry or molecular testing , depending on the laboratory. Ensure all testing is performed in accordance with GxP, GMP, SOPs and regulatory requirements . Review and approve analytical data, results, deviations, OOS/OOT investigations and laboratory documentation. Support method validation, method transfer, equipment … Requirements Previous experience leading a QC laboratory team within a pharmaceutical, biotech, medical device or other regulated environment. Strong knowledge of GMP/GxP and QC laboratory processes . Experience with investigations, deviations, OOS/OOT and CAPA. Understanding of analytical testing, laboratory systems and data integrity. Strong leadership, communication ...

field enablement across healthcare providers, medical devices, and biotech distributors. You will translate the platform's modular capabilities into compliant messaging (FDA/GxP/MDR) and craft trusted narratives for enterprise buyers while partnering with sales to accelerate deals. #J-18808-Ljbffr ...

skills across application, database, and integration layers. Practical SQL experience, including log and trace analysis. Understanding of manufacturing processes and MES operations within regulated (GxP) environments. Ability to work independently and drive issues through to resolution with minimal onboarding. Excellent communication skills and stakeholder management experience. Guidant, Carbon60, Lorien ...

Strong understanding of healthcare and life sciences workflows (e.g., drug discovery, clinical trials, regulatory submissions, market access) Familiarity with data privacy and compliance (HIPAA, GxP) Demonstrated ability to design and execute complex deal and partnership strategies You might thrive in this role if you: Are customer-centric and can translate ...

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 ...

biopharma clients. You will coach staff, ensure high-quality deliverables, and contribute to business development while maintaining strong client experience. You will bring GxP validation experience and a track record in R&D operations, leading teams to meet scope, schedule, and budget in a fast-paced environment. #J-18808-Ljbffr ...

design in a global neuroscience imaging platform. The successful candidate will guide policy development, partner with IT and CTO, and ensure adherence to GxP, GDPR, ISO standards and industry best practices. #J-18808-Ljbffr ...

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 ...

validated, audit-ready environments, drive platform upgrades and cloud evolution, and partner with senior leadership to deliver robust regulatory solutions. This role requires deep GxP experience and travel up to 15%. #J-18808-Ljbffr ...

intersection of Digital Technology, science, engineering, and business operations, ensuring that systems meet the highest standards of cybersecurity, data integrity, operational resilience, and GxP compliance.Who you'll work withYou will work closely with CMC Development Sciences scientists, Functional System Owners, business stakeholders, vendors, and Digital Technology colleagues to deliver reliable … define implementation roadmapsLead solution design and coordinate implementation, integration, qualification, validation, testing, and transition into operation for new and existing systemsEnsure systems comply with GxP, cybersecurity, quality, regulatory, and service management requirements while maintaining data integrity, resilience, and business continuityCollaborate with vendors, DT teams, and service component owners to resolve ...

strategy and collaborates with senior leaders to ensure compliant, scalable technology across GRAS. The role requires deep experience in regulatory operations, Veeva Vault, and GxP environments, with a track record of delivering robust, audit-ready solutions. #J-18808-Ljbffr ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

role Certified auditor Minimum 10 years auditing experience. At least 30 audits in one or more of these areas: Computer System Validation (CSV), IT GxP compliance, AI GxP compliance, electronic data integrity. Minimum 15 years in Pharma/Med Device industry Fluent in English and ideally one other EU language … applications. Experience in validation of multiple system delivery models including SaaS, PaaS, IaaS, and On Prem. Basic understanding of AI use cases and emerging GxP compliance requirements Experience in authoring policies and procedures (SOPs). Experience conducting audits and gap assessments. Experience managing internal personnel, contract resources, and projects. Expert ...

Technical Project Coordinator - Label Management, GxP/CSV Contract: 6 Months IR35: Inside IR35 Location: Remote Overview We are seeking a Technical Project Coordinator with experience in Label Management Systems, Computer System Validation (CSV), and regulated GxP environments to support a major label and artwork management implementation programme. The role … Label & Artwork Management or Label Management Systems (LMS), ideally Kallik (Veraciti/Veracity) or similar platforms. Strong understanding of Computer System Validation (CSV) within GxP-regulated environments Proven technical documentation skills, including creation of LLDs, validation documentation, runbooks, risk assessments, and operational handover materials. Knowledge of SAP integrations and label ...

cloud-based and regulated environments Driving audit readiness, compliance programs and evidence-based assurance across frameworks such as ISO 27001, GDPR, SOC 2 and GxP Providing leadership on risk management, governance and security strategy Partnering with customers, auditors and key stakeholders on security reviews, assurance activities and regulatory compliance Supporting … several of the following areas: Security leadership, governance, risk and compliance (GRC) Cloud security architecture and security strategy ISO 27001, GDPR, SOC 2, GxP, 21 CFR Part 11 or similar regulated frameworks Audit leadership, customer assurance and certification programs Healthcare technology, pharmaceutical, biotechnology or regulated SaaS environments Customer-facing security ...

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 ...

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 ...

performance, including obsolescence management and application of functional and safety standards Develop and maintain procedures for integration of IT and IACS systems in both GxP and non-GxP environments Support development of OT architecture, standards, and governance, and collaborate with global and local stakeholders Drive communication and change management within … Experience with industrial automation systems and OT architecture, including integration with IT systems Familiarity with regulated environments and standards such as GxP (including GMP and GAMP5) and IEC 61508/61511 Understanding of cyber security risk assessments, controls, and system documentation Experience in system lifecycle management, including validation, change control ...

teams. Together, you will ensure that technology solutions enhance productivity, maintain compliance, and support research innovation.What You’ll DoDefine and implement digital solutions for GxP lab automation and data managementOversee compliance of GxP IT systems, ensuring proper documentation and validationAct as the DT System Owner (DTSO … Engineering, Life Sciences, or a related fieldStrong technical affinity with IT systems and scientific instrumentation3+ years of experience in a similar role within GxP environmentsExperience in managing digital lab automation and research workflowsExperience with Modeling and Simulations tools, e.g. Nonmem, R, Python,...Knowledge of IT compliance frameworks (e.g., Computerized Systems ...

trial datasets.Quality & AI-Driven Compliance: Lead Test-Driven Development (TDD) and Behavior-Driven Development (BDD) initiatives. Use AI test generators to produce HIPAA/GxP-compliant synthetic clinical trial datasets for automated validation. Leverage AI tools to auto-draft validation artifacts, data lineage manifests, and audit documentation required under GxP … quality checks.Domain & Regulatory Awareness: Strong foundational understanding of clinical trial data workflows (e.g., EDC architectures), healthcare data models, and life science compliance standards (GxP, HIPAA, GDPR), with the ability to apply AI/ML tools for schema mapping and zero-loss data integrity verification.Base pay is one part ...