15 of 15 Remote/Hybrid Permanent GxP Jobs

analysis of system issues Report Development: Tools like: Data Analytics: Interpreting lab data and presenting insights Regulatory & Compliance Knowledge (Critical in LIMS) Understanding of: GxP (Good Practice standards) FDA 21 CFR Part 11 ISO 17025/GMP Knowledge of: Electronic signatures Audit trails Data validation processes On-premise and cloud ...

with both scientific and business audiences Familiarity with European data privacy and health data frameworks, including GDPR, the EU Health Data Space (EHDS) regulation, GxP requirements, and EMA guidance on AI/data-driven technologies Annual Salary £280,000—£330,000 GBP Logistics Minimum education Bachelor’s degree ...

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 ...

comparable regulatory systems experience will be considered. Strong requirements gathering, process mapping and stakeholder management skills. Agile experience, including user stories and backlog management. GxP/FDA or Computer System Validation experience would be advantageous. This is an excellent opportunity for a strong Regulatory Business Analyst to join a global ...

Data Protection Act**: Ensure all IT practices comply with data privacy regulations in the EU and UK.* **Pharma-Specific Regulations**: Familiarity with GxP (Good Practices) and other quality standards commonly required in the pharmaceutical industry. #J-18808-Ljbffr ...

within regulated industries , such as Life Sciences, Pharmaceuticals, Chemicals or Manufacturing PRINCE2, PMP, APM PMQ or equivalent project management qualification Desirable Experience Knowledge of GxP validation or validated system implementations Experience delivering global software rollouts across multiple sites Strong commercial awareness, including experience managing project financials, budgets and contract scope ...

projects within regulated industries such as Life Sciences, Pharmaceuticals, Chemicals or Manufacturing PRINCE2, PMP, APM PMQ or equivalent Project Management qualification Desirables Knowledge of GxP validation or validated system implementations Experience delivering global software rollouts across multiple sites Commercial awareness with experience managing project financials and contract scope The Company ...

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 ...

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/ ...

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 ...

cloud-based and regulated environments Driving audit readiness, compliance programs and evidence-based assurance across frameworks such as ISO 27001, GDPR, SOC 2 and GxP Providing leadership on risk management, governance and security strategy Partnering with customers, auditors and key stakeholders on security reviews, assurance activities and regulatory compliance Supporting … several of the following areas: Security leadership, governance, risk and compliance (GRC) Cloud security architecture and security strategy ISO 27001, GDPR, SOC 2, GxP, 21 CFR Part 11 or similar regulated frameworks Audit leadership, customer assurance and certification programs Healthcare technology, pharmaceutical, biotechnology or regulated SaaS environments Customer-facing security ...

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and ...

At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and ...

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 ...