26 to 44 of 44 GxP Jobs in London

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 At Syneos ...

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 ...

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 ...

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 ...

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 ...

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 ...

LIMS systems). The Role: You'll play a key role in maintaining and enhancing the organisation's Quality Management System, ensuring compliance with GxP regulations and supporting continuous improvement across the business. You will be also supporting with regulatory training, eQMS and QA projects. Responsibilities: Planning and conducting internal … essential. Strong experience auditing GCP clinical sites and CSV (Computer System Validation). Experience supporting regulatory inspections and external audits. Good understanding of GxP regulations and quality systems.Why Apply? Join a leading UK biotechnology organisation making a real impact. Hybrid working (2/3 days on-site). Competitive salary ...

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 ...

features across asset teams; contracting vendors on outcomes and holding teams to account for quality, pace and measurable value. Embed quality, risk and compliance , GxP, privacy and AI governance, from the outset, ensuring transparent, auditable platforms and good hygiene in core systems of record. Build trusted partnerships and influence … building high-performing product teams. Experience delivering AI, data and analytics-enabled products on modern data platforms and cloud technologies. Experience operating in a GxP/validated-systems context, with strong data integrity, quality and compliance judgement. Preferred Qualifications Deep experience with structured content management, modular document design or publications ...

Join us as a Senior IT Quality & CSV Specialist. As Senior IT Quality & CSV Specialist you will provide independent quality and validation oversight for GxP computerised systems and complex global IT projects within a pharmaceutical environment. You will work with project teams, system owners, IT teams and regulated business functions … ensure computer system validation activities are risk-based, compliant with global regulatory requirements, and inspection-ready. What you'll do: Provide quality oversight of GxP computerised systems throughout the full validation lifecycle. Review validation documentation including Validation Plans, Validation Reports, requirements, traceability matrices, design documentation, test plans, test reports, testing ...

Join us as a Senior IT Quality & CSV Specialist. As Senior IT Quality & CSV Specialist you will provide independent quality and validation oversight for GxP computerised systems and complex global IT projects within a pharmaceutical environment. You will work with project teams, system owners, IT teams and regulated business functions … ensure computer system validation activities are risk-based, compliant with global regulatory requirements, and inspection-ready. What you'll do: Provide quality oversight of GxP computerised systems throughout the full validation lifecycle. Review validation documentation including Validation Plans, Validation Reports, requirements, traceability matrices, design documentation, test plans, test reports, testing ...

test design, defect triage, and release confidence.Working knowledge of regulatory and compliance expectations relevant to software quality in regulated environments, including FDA, GDPR, and GxP principles.Excellent communication and presentation skills; able to craft executive-ready narratives and influence decisions.Candidate Profile – PreferredExperience in regulated environments (medical devices/healthcare) with working … knowledge of FDA expectations, GDPR, GxP, and risk-based validation approaches such as CSA.Salesforce certifications (e.g., Salesforce Administrator, Platform App Builder, or related certifications) and/or experience supporting Salesforce release management and platform upgrades.Certifications or demonstrated experience in automation engineering, Selenium/Java ecosystems, enterprise application testing, or ISTQB ...

laboratory supplies, and biotech distribution. You will translate commercetools’ modular flexibility into trust-building messaging that addresses regulatory compliance (FDA 21 CFR Part 11, GxP,MDR), audit trail requirements, data security, and complex healthcare procurement processes. Vertical Positioning & Messaging: Develop and execute the GTM strategy for MedTech & Life Sciences, framing … including 3+ years deeply focussed on the HealthTech, MedTech & Life Sciences sectors. Clear understanding of healthcare procurement, medical device distribution, and regulatory frameworks (FDA, GxP, HIPAA, MDR). This includes 3+ years experience deeply focussed on the Industrials & Manufacturing industry sector. Strong ability to craft compelling, trust-building narratives ...

fully aligned, informed, and motivated to achieve world-class results Requirements Extensive program leadership experience (7+ years) delivering enterprise-scale R&D or GxP technology programs in Pharma (Clinical, Regulatory, or Safety) Deep understanding of Pharmaceutical R&D functions such as Clinical Operations, Regulatory Affairs, Safety, Quality, or Manufacturing Proven … Veeva Vault implementation (e.g., Clinical, RIM, Quality, Safety) Previous experience with large-scale Software as a Service (SaaS) implementations in the highly regulated GxP environment Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity ...

Amgen is seeking a Senior Manager, Instructional Designer to lead and shape training across GxP learning programs. You will drive material development, curricula, and assessment design to support regulatory compliance and product quality. You will collaborate with governance and subject-matter experts, ensuring content accuracy, accessibility, and end-user usability. ...

strategies across global programmes. Influence development programs through AI innovation, clinical development, operations, regulatory compliance, and commercialisation. Hands-on with QMS improvement and full GxP compliance. Support CTA, IND, IMPD, MAA and broader regulatory submission activities. Lead cross-functional programmes spanning Regulatory Affairs, Quality, Clinical Development and AI teams. Partner … frameworks. Strong understanding of drug development and global regulatory pathways. Experience supporting CTA, IND, IMPD, and marketing application activities. Hands-on experience with GxP, Quality Systems and regulatory compliance. Ability to work effectively across AI, scientific, regulatory and development teams. Experience within gene therapy, AAV, neuroscience or CNS programmes ...

Amgen is seeking a Sr Manager, Instructional Designer to partner with Governance and drive effective GxP Learning programs. You will design instructor-led, virtual, e-learning, blended learning, and performance-support materials, translating complex regulated content into clear training solutions. You will lead curriculum development, ensure regulatory compliance, assess outcomes ...