26 to 50 of 84 GxP Jobs in the UK

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 ...

Strong interpersonal skills with the confidence to articulate technical concepts, present ideas, and engage directly with senior business leaders.(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 packageBuilding ...

strategies to 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 ...

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 ...

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 ...

lifecycle — from early research through to commercial supply.We are seeking an experienced Pharma Quality SpecialistConsultant to join our Life Sciences consulting team, specialising in GxP Quality Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with … client engagements, applying your quality expertise to deliver tangible impact. Your work will include:QMS design and process transformationLeading the design and implementation of GxP‐compliant QMS across R&D, manufacturing, clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned ...

lifecycle — from early research through to commercial supply.We are seeking an experienced Pharma Quality SpecialistConsultant to join our Life Sciences consulting team, specialising in GxP Quality Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with … client engagements, applying your quality expertise to deliver tangible impact. Your work will include:QMS design and process transformationLeading the design and implementation of GxP‐compliant QMS across R&D, manufacturing, clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned ...

Position Summary The Computer System Validation (CSV) Specialist is responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical … inspection readiness and data integrity. Essential Functions Own and maintain the site Computerised Systems Validation (CSV) Master Plan. Manage the full validation lifecycle of GxP systems (URS, risk assessment, IQ/OQ/PQ, validation reports). Assess and approve system updates, configuration changes, and upgrades in line with change ...

translate global security standards into local implementation and advance secure IT/IACS integration across sites. With experience in OT cyber security, GMP/GxP, and IEC standards, you will lead risk assessments, lifecycle management, and project delivery while collaborating with global and local stakeholders to ensure #J-18808-Ljbffr ...

systems. The role is remote with an initial 6-month contract for a high-impact life sciences programme, requiring extensive experience in GMP/GxP and cybersecurity within #J-18808-Ljbffr ...

Good compliance understanding of industry domains such as BFSI – (SOX, FFIEC, PCI-DSS, BASEL, MAS etc.), Healthcare & Life-sciences – (HIPAA, Hi-Trust, FDA CFR, GxP Compliance), Telecom, Retail, Data Privacy (GDPR, CCPA) Energy & Utilities (NERC, FERC) Information Security (ISO 27000, NIST, CIS) TPRM • Business Resiliency & Cyber Recovery, ZTA • GRC Project ...

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 ...

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 ...

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 ...

improvement of the Company’s IT infrastructure. The IT Analyst role ensures the availability, reliability, security and compliance of IT systems supporting business and GxP activities. Working within a regulated environment, the position contributes to computer system validation, cybersecurity, data integrity, audit readiness and regulatory compliance. Your Responsibilities Infrastructure & Network … requests, problems and changes using ITIL principles. Maintain SLA performance and perform root cause analysis for recurring issues. Maintain IT asset and configuration records. GxP Compliance and Validation Responsibilities Support validated and regulated computer systems throughout their lifecycle. Participate in user requirements gathering, risk assessments, validation planning and test execution. ...

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 ...

computerised-system lifecycle in Stevenage. You will partner with Quality, Manufacturing, Engineering and IT to deliver compliant CSV solutions across GxP operations in CAR‐T cell therapy manufacturing. The role requires 5+ years in validation, strong GAMP5 knowledge, data integrity and regulatory-inspection experience, plus excellent technical writing and cross ...

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 ...

will bring a strong background in IT infrastructure, Windows Server, AD/GP, and virtualization (VMware/Hyper-V), with experience in regulated environments (GxP) being a plus. Expect 36-hour weeks and an on-site presence in Haverhill. #J-18808-Ljbffr ...

Kafka, develop backend services in Java or Scala on AWS, and apply AI-assisted tooling for schema mapping, testing, and validation, while ensuring GxP, HIPAA and GDPR compliance. #J-18808-Ljbffr ...

with architectural best practices. Key Responsibilities: Build and optimise scalable data pipelines using Databricks and Apache Spark (PySpark). Ensure performance, scalability, and compliance (GxP and other standards). Collaborate on requirements, design, and backlog refinement. Promote engineering best practices including CI/CD, code reviews, and testing. Research ...

with architectural best practices. Key Responsibilities: Build and optimise scalable data pipelines using Databricks and Apache Spark (PySpark). Ensure performance, scalability, and compliance (GxP and other standards). Collaborate on requirements, design, and backlog refinement. Promote engineering best practices including CI/CD, code reviews, and testing. Research ...

another regulated environment. Familiarity with document management or OCR tools. Experience using Jira and Confluence. Awareness of clinical governance or quality frameworks (for example GxP, ISO 13485, DCB0129/0160). What success looks like in the first 6 months Full ownership of e-sign configuration and first-line troubleshooting ...

regulatory requirements into practical, compliant solutions that support innovation Quality Management & Digital (QM&D) is responsible for the Innovative Medicine Quality Management System (IMQS), GxP ownership, and global Quality Management processes. Within QM&D, the Process & Data Management (PDM) team works with partners across Therapeutic Areas, Global Development, Global Regulatory … solutions that support business needs throughout the development lifecycle.In this role, you will contribute to improvement and compliance programs that require expertise across the GxP Quality Management System. Activities include Adopting Regulatory Requirements (ARR), Quality Framework integration, and strategic R&D Quality initiatives. The position evaluates, compares, maps, and integrates ...