101 to 125 of 239 GxP Jobs in the UK

will be responsible for providing administrative support for the Product Development/QMS team to maximise quality and efficiency and ensure compliance with relevant GxP regulations (GMP, GDP, GCP and GVP). Job Interactions & Interface: This role interacts internally with key areas such as Regulatory – CMC, Clinical and Product Development More ❯

or GAMP 5 (preferred) Knowledge, Skills, and Abilities Experience with ETQ, MasterControl, or similar eQMS platforms (configuration, administration, training) Strong knowledge of CSV and GxP system implementations in regulated environments Hands-on CSV activities with Empower CDS, including validation, data migration, archiving, audit trails, user access, data integrity Success in More ❯

modern infrastructure principles (e.g., Infrastructure-as-Code) Change management methodologies (e.g., Prosci, ADKAR, or equivalent frameworks) Security, privacy, and compliance in regulated environments (e.g., GxP, GDPR, ISO 27001) Full-stack software development principles (front-end, back-end, APIs, integration patterns) Systems reliability engineering (SRE), observability, and monitoring practices Data management More ❯

on experience with software implementation Proven ability to work both independently and in teams in a fast-paced environment Good understanding of SaaS and GxP principles Ability to quickly understand business requirements and design creative solutions Excellent verbal and written communication skills Bachelor’s degree or equivalent relevant experience Nice More ❯

building enterprise solutions, capturing requirements, and documenting business needs. Experience leading and managing development efforts to deliver client-facing solutions. Possess and understanding of GxP standards and application to systems involved in clinical studies. Experience managing vendors that include keeping efforts on track and negotiating agreements for development work. Ability More ❯

building enterprise solutions, capturing requirements, and documenting business needs. Experience leading and managing development efforts to deliver client-facing solutions. Possess and understanding of GxP standards and application to systems involved in clinical studies. Experience managing vendors that include keeping efforts on track and negotiating agreements for development work. Ability More ❯

with an end-to-end digital transformation platform. We combine our purpose-built systems with world-class consulting services to help every facet of GxP meet evolving regulations and quality expectations. The Team You’ll Join Our customers’ success is our success. We keep the customer experience centered in our More ❯

or equivalent Agile certification Agile delivery frameworks and tools (Scrum, Kanban, SAFe; Jira, Confluence, Azure DevOps) Security, privacy, and compliance in regulated environments (e.g., GxP, GDPR, ISO 27001) Application If you are interested in the role, please register your details, including a copy of your CV. Please note, while we More ❯

understanding Experience with the Tulip platform Supporting and maintaining IT systems such as MES and SAP ECC Applicants should have life sciences or GxP experience from industries like manufacturing or medical devices. For more information, contact Chanel Hicken at 0203 868 1011 or via email at chanel.hicken@planet-pharma.co.uk to More ❯

ECM platforms (e.g., Veeva Vault), migration tools, SQL, XML, scripting, cloud and on-premise solutions. Regulatory Knowledge: Understanding of life sciences regulations, validation, and GxP compliance. Leadership Abilities: Proven leadership in technical teams and project management, with strong problem-solving skills. #J-18808-Ljbffr More ❯

Proficiency in ECM platforms (e.g., Veeva Vault), migration tools, SQL, XML, scripting, cloud/on-prem solutions. Regulatory Knowledge: Understanding of life sciences regulations, GxP validation, and compliance. Leadership Abilities: Proven leadership in technical teams and project management, with strong problem-solving skills. #J-18808-Ljbffr More ❯

OpenText Documentum), migration tools, SQL, XML, scripting. Experience with cloud and on-premise solutions. Regulatory Knowledge: Understanding of life sciences regulations, validation processes, and GxP compliance. Leadership Abilities: Proven leadership in technical teams and project management, with strong problem-solving skills. #J-18808-Ljbffr More ❯

platforms (e.g., Veeva Vault, OpenText Documentum), migration tools, SQL, XML, scripting languages, and cloud/on-prem solutions. Strong understanding of life sciences regulations, GxP compliance, validation processes, and documentation. Proven leadership in technical teams and complex project management with excellent problem-solving skills. #J-18808-Ljbffr More ❯

experience (Veeva Vault, OpenText, Generis CARA), migration tools, SQL, XML, scripting, cloud/on-premise solutions. Regulatory Knowledge: Understanding of life sciences regulations, validation, GxP compliance. Leadership Abilities: Proven leadership in technical teams and project management, with strong problem-solving skills. #J-18808-Ljbffr More ❯

Veeva Vault, OpenText Documentum, Generis CARA), migration tools, SQL, XML, scripting, cloud/on-premise solutions. Regulatory Knowledge: Understanding of life sciences regulations, validation, GxP systems, and compliance. Leadership Skills: Proven leadership in technical teams and project management, with strong problem-solving abilities. #J-18808-Ljbffr More ❯

OpenText Documentum, Generis CARA), migration tools, SQL, XML, scripting languages, and cloud/on-premise solutions. Strong understanding of life sciences regulations, validation, and GxP compliance. Proven leadership in technical teams and complex project management, with excellent problem-solving skills. #J-18808-Ljbffr More ❯

ensure standards and alignment. (10%) Provide technical oversight for enterprise-level IT/OT systems, evaluate project work, staff, and procedures. Prepare documentation for GxP and critical IT technologies, participate in validation and testing, and represent IT in audits. (40%) Consult with system administrators, vendors, and other departments to guide More ❯

risk management information to Key Stakeholders throughout the Product Lifecycle. Requirements Master’s degree in scientific discipline with a few years of experience in GxP within pharmaceutical industry Proficient experience with clinical trials, clinical research associate, clinical trial management, or clinical auditing considered a plus Proven knowledge in Project Management More ❯

Good spoken and written skills. - Proactive approach to problem solving. Desirable Skills/Experience - Exposure to Run SAP (Solution Manager) methodologies. - Good understanding of GXP and SOX requirements. Should have working experience in a validated environment. At AstraZeneca, we empower our teams to motivate change across international boundaries, fostering an More ❯

teams. Deep experience in life sciences, pharmaceutical workflows, or scientific research environments—especially related to drug discovery, biologics, automation, or emerging modalities. Background in GxP compliance or familiarity with Good Laboratory Practices (GLP). Bachelor’s degree in Computer Science, Chemistry, Business, or a related field (or equivalent work experience More ❯

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 More ❯

3+ years of experience in Life Sciences, Healthcare, or an adjacent Safety industry Experience implementing, supporting, or administrating core business/IT operations with GxP software solutions Good knowledge of implementation methodologies for SaaS solution Proven ability to deliver on time and with a high degree of satisfaction Longstanding passion More ❯

information confidentially and professionally. Capable of working independently and managing multiple priorities. Right to work in the UK. Preferred Attributes: Experience supporting GMP/GxP or other regulated environments. Familiarity with construction/engineering document lifecycles and transmittal processes. Strong interpersonal skills and a proactive, team-oriented attitude. Willingness to More ❯

maintaining asset inventories. The discipline to produce and follow detailed technical documentation for tasks and projects. Experience within Regulated environments such as ISO27001 or GxP is Beneficial Strong troubleshooting skills and the ability to plan and estimate tasks. Knowledge of IT frameworks, such as ITIL, Kanban Lean IT or Agile More ❯

real-world evidence generation, biomarker discovery). Regulatory & Compliance Oversight: Ensure data practices adhere to FDA, EMA, GDPR, HIPAA, and industry standards (e.g., CDISC, GxP). Data Governance & Architecture: Oversee the design of robust data ecosystems, including cloud platforms (AWS/Azure), data lakes, and governance frameworks to ensure quality More ❯