Stoke-on-Trent, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
documents, risk management plans, and post-project reviews. Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR). Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services. Support More ❯
Newcastle upon Tyne, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
documents, risk management plans, and post-project reviews. Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR). Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services. Support More ❯
Hull, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
documents, risk management plans, and post-project reviews. Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR). Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services. Support More ❯
Manchester, England, United Kingdom Hybrid / WFH Options
JR United Kingdom
documents, risk management plans, and post-project reviews. Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR). Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services. Support More ❯
dynamic, and high-pressure environment. Commitment to maintaining high standards of quality and compliance. Cold chain and temperature management experience. Understanding and familiarity with GxP principles. Data collection and analytical skills with a commitment to data integrity. Commitment to continuous improvement initiatives with the ability to learn, grow, and adapt More ❯
Foster a culture of continuous improvement through the adoption of emerging technologies. Cybersecurity and Compliance Ensure IT systems align with global regulatory requirements (e.g., GxP, FDA, and EMA standards) and local data protection laws. Adhere to and implement robust cybersecurity measures to protect sensitive data and ensure business continuity. Conduct More ❯
skills, both written and verbal Attention to detail and commitment to quality excellence Preferred Skills Experience with automated testing frameworks and tools Knowledge of GxP, 21 CFR Part 11, or ISO 13485 standards Background in clinical data validation or laboratory testing environments Familiarity with electronic health record (EHR) systems Experience More ❯
skills, both written and verbal Attention to detail and commitment to quality excellence Preferred Skills Experience with automated testing frameworks and tools Knowledge of GxP, 21 CFR Part 11, or ISO 13485 standards Background in clinical data validation or laboratory testing environments Familiarity with electronic health record (EHR) systems Experience More ❯
Skills: 10+ years SAP project management experience with multiple full-cycle rollouts. Background in life science or pharmaceutical industries. Strong knowledge of cGMP/GxP compliance and regulatory environments. Excellent leadership, communication, and stakeholder management skills. Additional Information At Fusion, we aspire to be one of the world's leading More ❯
field, or equivalent work experience. Strong experience in agile environments, particularly in customer-facing deployments. Knowledge or experience in Life Sciences, Pharma workflows, or GxP compliance-related activities is a plus. Competitive Salary and equity in a fast-growing company. Generous Paid Time Off (PTO) and wellness benefits. Flexible Working More ❯
London, England, United Kingdom Hybrid / WFH Options
Jobgether
field, or equivalent work experience. Strong experience in agile environments, particularly in customer-facing deployments. Knowledge or experience in Life Sciences, Pharma workflows, or GxP compliance-related activities is a plus. Competitive Salary and equity in a fast-growing company. Generous Paid Time Off (PTO) and wellness benefits. Flexible Working More ❯
Hook, England, United Kingdom Hybrid / WFH Options
Elanco
Strong experience with agile methodologies, DevSecOps practices, and modern engineering frameworks. Strong grasp of data privacy, security and compliance in a global context (GDPR, GxP, SOX). Excellent communication and stakeholder management skills with the ability to influence across cross-functional teams. A deep commitment to technical excellence and an More ❯
Hart, Yorkshire, United Kingdom Hybrid / WFH Options
Elanco Tiergesundheit AG
Strong experience with agile methodologies, DevSecOps practices, and modern engineering frameworks. Strong grasp of data privacy, security and compliance in a global context (GDPR, GxP, SOX). Excellent communication and stakeholder management skills with the ability to influence across cross-functional teams. A deep commitment to technical excellence and an More ❯
Hartley Wintney, England, United Kingdom Hybrid / WFH Options
Elanco Tiergesundheit AG
Strong experience with agile methodologies, DevSecOps practices, and modern engineering frameworks. Strong grasp of data privacy, security and compliance in a global context (GDPR, GxP, SOX). Excellent communication and stakeholder management skills with the ability to influence across cross-functional teams. A deep commitment to technical excellence and an More ❯
involved with internal inspections and external customer audits, identifying Quality risks and implementing any required mitigating actions, and the delivery of relevant system and GxP training to the business to maintain our strong QA culture. The Person Experience of working with Pharmaceutical Quality Systems; an understanding of Quality regulations would More ❯
/OQ/PQ, SOPs, etc.) Provide training and ongoing support to system users and stakeholders Ensure systems remain audit-ready and compliant with GxP, GLP, and CSV requirements Act as SME for validated systems and support continuous improvement Manage archiving processes and act as GLP archivist Communicate project progress More ❯
IVDD 98/79/EC; IVDR 2017/746 and other appropriate regulations and standards. This includes site safety requirements and applicable GxP and Good Manufacturing Practices (GMP). Key Responsibilities: Management and development of robust and compliant validation processes and procedures to include maintenance, development and execution of More ❯
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 ❯
Skills, and Abilities Proven experience working with ETQ, MasterControl, or similar eQMS platforms – configuration, administration, and user training Strong working knowledge with CSV and GxP system implementations in a regulated pharmaceutical or life sciences environment Hands-on experience with CSV activities relating to Empower CDS, including: Validation of new Empower More ❯
Skills, and Abilities Proven experience working with ETQ, MasterControl, or similar eQMS platforms – configuration, administration, and user training. Strong working knowledge with CSV and GxP system implementations in a regulated pharmaceutical or life sciences environment. Hands-on experience with CSV activities relating to Empower CDS, including: Validation of new Empower 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 ❯
London, England, United Kingdom Hybrid / WFH Options
Veeva Systems
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 ❯