1 to 25 of 80 GxP Jobs in the UK

storage and endpoint management solutions Experience working within a pharmaceutical, biotechnology, medical device or similarly regulated environment would be highly desirable An understanding of GxP, GMP, GAMP 5, Annex 11 and 21 CFR Part 11 would be advantageous Strong understanding of IT service management and ITIL principles Excellent analytical ...

configure and customise an ELN (Benchling preferable) or comparable laboratory informatics platform, including schemas, modules and custom workflows. Understanding of regulatory standards including GxP, ALCOA+ principles, and 21 CFR Part 11 requirements. Desirable: Knowledge and understanding of the cell and gene therapy industry. Experience designing and implementing system integrations using ...

professional who thrives in a project-based environment. You will be responsible for the planning, execution, and management of commissioning and qualification activities for GxP-regulated facilities (Pharma, Biotech, and Medical Devices). Responsibilities include, but are not limited to: Project Execution: Lead and execute C&Q strategies for process ...

primary business owner for the platformPartner with Biometrics, Data Science, IT, Quality, and external vendors to ensure platform reliability, compliance, and business value.Ensure GxP compliance, validation, inspection readiness, and data integrity requirements.Translate clinical analysis and reporting requirements into scalable platform capabilities supporting regulatory submissions and evidence generation.Drive adoption of modern ...

improvement across the department. About You A relevant Biochemistry, Biomedical, or other applicable science-based degree At least 4 years' laboratory experience in a GxP environment, including 2 years in a management capacity At least 4 years' experience working with HPLC, UPLC, and LC-MS/MS, with frequent ...

pharmaceutical discipline. Minimum of 5 years’ regulatory experience, ideally within radiopharmacy, sterile manufacturing or aseptic processing. Proven experience with GMP, MHRA expectations and broader GxP requirements. Experience supporting commercial and IMP product development, including clinical trial supply. Strong understanding of regulatory inspections and authority interactions. Experience working across multi‐site ...

improvement across the department. About You A relevant Biochemistry, Biomedical, or other applicable science-based degree At least 4 years' laboratory experience in a GxP environment, including 2 years in a management capacity At least 4 years' experience working with HPLC, UPLC, and LC-MS/MS, with frequent ...

single platform or technology. Experience working in complex, cross-functional enterprise environments. Experience with cloud-based data and integration architectures. Experience with regulated/GxP environments preferred. Skills/Specialist Knowledge Strong knowledge of enterprise data architecture and solution architecture principles. Advanced data modeling skills, including conceptual, logical, dimensional ...

careers/orion-as-an-employer/. We are seeking an individual with experience in pharma or industrial environments, including an understanding of GxP compliance and IT support in regulated environments. Skills & Qualifications: Technical Proficiency: Windows, macOS, Microsoft 365, Active Directory, VPN, remote desktop tools, and enterprise applications. Customer ...

with infrastructure considerations (networking, hosting, security, etc.) in enabling on-premise and cloud IT solutions. Knowledge of data integrity and compliance standards within a GxP-regulated environment (e.g., 21 CFR Part 11). Solution architecture certifications for Microsoft Azure or Google Cloud Platform. Experience working in a product operating model ...

skills. Experience managing suppliers or third-party service providers. Experience within regulated industries such as life sciences, pharmaceuticals, biotechnology, or clinical research. Knowledge of GxP, ISO 27001, or similar compliance frameworks. Relevant Microsoft, Citrix, VMware, or security certifications. Personal Attributes Collaborative and approachable leadership style. Able to balance strategic thinking ...

teams (e.g., bioinformatics, wet lab, clinical research) Experience designing systems that manage laboratory or bioinformatics data (e.g., LIMS, sequencing pipelines, assay metadata) Familiarity with GxP practices and regulatory reporting requirements in clinical studies is a plus Prior experience working in biotech, diagnostics, or life sciences companies Experience supporting sample tracking ...

CSL Vifor is seeking a Quality Systems professional to support GMP-compliant quality systems across validation, calibration and document management. You will contribute to internal audits and continuous improvement programs while ensuring alignment with FDA ...

equipment issues, supporting CAPA activities. Assist with installation, commissioning, qualification and validation activities, including IQ/OQ/PQ. Ensure compliance with GMP, GxP and ALCOA+ data integrity requirements. Analyse data from serialisation, automation and production systems to identify opportunities for performance improvement. Support and maintain PLCs, HMIs, scanners, printers ...

Engineering or a related field. Significant’ experience in a Systems Analysis, Business Analysis or related analytical role. Experience of software delivery activities within a GxP/pharmaceutical/other regulated environment. Demonstrable experience of leading, supervising or line-managing a team of analysts or related professionals. A record of being ...

Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability to quickly understand business requirements and design creative solutions Excellent verbal and written communication skills Experience in the Life Sciences Quality, Manufacturing, or Healthcare spaces ...

software implementation Excellent verbal and written communication skills and the ability to engage with senior/executive‐level stakeholders Good understanding of SaaS and GxP principles Ability to travel 25-50%; easy access to an airport Must be legally authorized to be employed in the EU. Veeva Systems does ...

projects. Familiarity with common enterprise services (Directory Services, Information Assurance, Identity and Access Management, etc.), products (i.e., Oracle, SAP) and frameworks (ITIL, Zachman, TOGAF, GxP, HIPAA, etc.) Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions ...

mindset, make resource trade-offs, and drive measurable commercial outcomes. Navigate the tension between speed-to-market and regulatory compliance (GxP, 21 CFR Part 11, GDPR, HIPAA). Cultivate strategic partnerships with data providers and standards bodies (CDISC, HL7 FHIR) to accelerate Evinova's product capabilities. Champion a culture ...

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 ...

data formats and quality challenges Ability to work effectively and cross-functionally with data science, data engineering, legal, commercial and product teams Familiarity with GxP/regulated software environments Even better if you have experience of... Healthcare, biotech, medtech, or techbio environments Experience in high-growth startups or scaleups Familiarity ...

type of person who loves experimenting, learning new frameworks, or building side projects in your spare time. (Bonus: Experience or familiarity with GxP/GDPR or the Pharmaceutical industry is a nice-to-have, but certainly not a dealbreaker!) What we offer in return Flexible benefits package Opportunities for learning ...

willingness to travel up to 40% for customer meetings and presentations Nice to Have Quality & Manufacturing Domain Expertise: Industry experience spanning Quality Control (QC), GxP quality content, training management, quality systems processes, or manufacturing Commercial Leadership: Proven experience leading or guiding global sales teams to aggressively pursue and close complex ...

Pharmaceutical or Life Sciences industryFunctional knowledge of Clinical, Regulatory, Quality, or Safety business processesPrevious Project Management exposure for complex enterprise software implementationsFamiliarity with GxP and software validation regulationsDeep understanding of the migration verification and reconciliation processCoding experience, particularly with Java or PythonInterviewing with VeevaWe value your time and believe ...

Senior C&Q Consultant/Engineer to join our UK Field Services team. You will plan, execute, and manage commissioning and qualification activities for GxP-regulated facilities in Pharma, Biotech and Medical Devices. Travel to client sites is a core aspect of the role. Ideal candidates have deep ...