1 to 25 of 35 Permanent GxP Jobs in England

to develop strong relationships across global teams. Experience in IT Project Management. Experience with Agile ways of working. General knowledge of the pharmaceutical setting (GXP, Validation, Privacy Concerns, ). Experience with or interest in machine learning or statistical methods. Stakeholder-facing skills to set expectations and communicate effectively. Successfully managing More ❯

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 ❯

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 ❯

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 ❯

multidisciplinary technical oversight, including evaluation of project work, staff, methods, and procedures related to enterprise-level IT/OT systems. Compile technology documentation for GxP and critical IT technologies. Participate in system validation and testing, approve validation documentation with ITQ, and represent IT systems during audits and inspections. (40%) Consult More ❯

adhered to with handling, processing, security & privacy of data, compliant with internal security, risk management policies and practices, external regulatory and statutory requirements e.g., GxP, Sarbanes Oxley and that Tech continuity plans are in place for all business-critical products. Build relationships both internally & externally, collaborating closely with technologists and More ❯

team. Who you are: Degree in Engineering or significant technical/quality service background. Familiarity with 21 CFR Part 11, GAMP 5, Annex 11, GxP, and other regulatory standards. Minimum of 4 years of experience in associated field. Ability to understand and interpret technical product documentation. Experience working within a More ❯

with PM and FICO modules. Background in life scienceor pharmaceutical industries (maximum during the most recent 5-7 years) Strong knowledge of cGMP/GxP compliance and regulatory environments, with a minimum of 2 years hands-on experience with GxP. Experience ensuring cGMP compliance for validation, change management, and documentation. More ❯

Life science manufacturing - GAMP 5 understanding Tulip platform Supporting & maintaining IT business systems such as MES, SAP ECC You must have life sciences or GxP experience from similar industries such as manufacturing or medical devices etc. For more information on this position or any similar opportunities, please contact Chanel Hicken More ❯

resolving general networking issues. Experience: Extensive IT/Commercial experience gained within a fast-paced environment? Experience of GAMP 5 and working within a GxP environment in providing superior customer service and support. Experience of working within a technical support position, covering Windows, Microsoft Office, Internet Explorer and various business More ❯

Quality System documents and procedures relevant to all employees (local and Convatec corporate e.g. Code of Ethics and Business Conduct, Quality Policy, Complaints, relevant GxP documents), including regular re-training when required. Quality System documents and procedures relevant to job performance. Principal Contacts & Purpose of Contact: Internal: Global T&I More ❯

advisory roles, with significant exposure to the medical, life sciences, or pharmaceutical industry. Demonstrated knowledge of regulatory processes, medical content lifecycle, and compliance frameworks (GxP, HIPAA, ABPI, etc.). Proven experience working with or consulting on: Veeva Vault Medical Suite Salesforce (Health Cloud or Life Sciences verticals) Adobe Experience tools More ❯

On-Demand sector to ensure compliance with regulatory, customer and other relevant standards as applicable. Provide guidance and support the business to ensure existing GxP regulations are adhered to throughout the project for example, supporting change management and periodic reviews. Support the delivery of the Uniphar On-Demand sector quality More ❯

storage, and backup technologies. Adherence to change management and global IT policies. Strong troubleshooting skills and technical documentation discipline. Experience in regulated environments (ISO27001, GxP) is beneficial. Knowledge of IT frameworks such as ITIL, Agile methodologies; Linux knowledge is a plus. Soft Skills and Qualifications: Ability to work independently and More ❯

to 10% Nice to Have Experience in the pharmaceutical and life sciences industry Experience with Clinical, Regulatory, Quality, or Safety business processes Experience with GxP regulations and software validation process Document/Data migration experience Experience with source code control systems Amazon Web Services (AWS) tools such as Lambda and More ❯

and adherence to global policies and procedures. Experience maintaining asset inventories. Ability to produce and follow detailed technical documentation. Experience in regulated environments (ISO27001, GxP) is beneficial. Strong troubleshooting skills and task planning abilities. Knowledge of IT frameworks such as ITIL, Kanban, Lean IT, or Agile. Knowledge of Linux is More ❯

Risk & Compliance: Support operational technology compliance with internal security and risk management policies and practices, as well as external regulatory and statutory requirements e.g. GxP and that Tech continuity plans are in place for all critical areas. People Management: Collaborate with internal owners of security technologies such as antivirus, IDS More ❯

problem areas Evidence of experience of the management of change Active management of plant changes in a controlled and safe way Understanding of what GxP and ALCOA are Monitoring and reviewing engineering progress with Project Services and Engineering disciplines Ability to be a focal point for assigned projects, managing issues More ❯

We are seeking a Business Systems Analyst with a strong background in regulated GxP environments , GAMP 5 guidelines , and experience working with SAP or MES ERP systems . The ideal candidate will play a crucial role in analyzing, designing, and optimizing business systems to ensure compliance, efficiency, and operational excellence … within a validated environment. Key Responsibilities: System Analysis & Optimization: Assess current business processes and system functionalities to identify areas for improvement and optimization. GxP Compliance & Validation: Ensure all business systems adhere to GxP regulatory requirements, with a focus on GAMP 5 best practices for system validation. ERP System Management: Support … ensure alignment on system requirements. Required Qualifications & Experience: Bachelor's degree in Computer Science, Business, Engineering , or related field. Proven experience working in a GxP-regulated environment within pharmaceuticals, life sciences, or biotechnology . Strong knowledge of GAMP 5 guidelines and system validation processes. Hands-on experience with SAP or More ❯

is seeking a QA Compliance Manager for a 12 month Fixed Term Contract. This role will lead and ensure that IT systems critical to GxP operations comply with regulations. You will be part of a supportive team focused on maintaining high standards in quality management and data integrity. Please note … that to be considered for this role you must have the right to work in this location. Responsibilities: Ensure IT systems meet GxP compliance standards. Support adherence to manufacturing and data integrity regulations. Oversee system validation and compliance processes. Review and manage changes to IT systems. Provide guidance on data … and Requirements: Previous experience within pharmaceuticals or biotechnology companies Must have previous experience in data integrity and system validation. Knowledge of IT compliance and GxP systems. Strong communication and stakeholder management skills. Proficient in using Word and Excel for data analysis. Detail-oriented with excellent report writing skills. Ability to More ❯

is seeking a QA Compliance Manager for a 12 month Fixed Term Contract. This role will lead and ensure that IT systems critical to GxP operations comply with regulations. You will be part of a supportive team focused on maintaining high standards in quality management and data integrity. Please note … that to be considered for this role you must have the right to work in this location. Responsibilities: Ensure IT systems meet GxP compliance standards. Support adherence to manufacturing and data integrity regulations. Oversee system validation and compliance processes. Review and manage changes to IT systems. Provide guidance on data … and Requirements: Previous experience within pharmaceuticals or biotechnology companies Must have previous experience in data integrity and system validation. Knowledge of IT compliance and GxP systems. Strong communication and stakeholder management skills. Proficient in using Word and Excel for data analysis. Detail-oriented with excellent report writing skills. Ability to More ❯

in cross-module functionalities to drive end-to-end business process efficiency. Ability to design, configure, and troubleshoot SAP FICO processes in a validated (GxP-compliant) environment. Experience in release management, ensuring high-quality system enhancements and changes. Drive system documentation excellence in compliance with GxP and other regulatory requirements. More ❯

Overview: This is a senior site-based quality role with responsibility for managing and developing the Quality Management System to ensure full GxP compliance. As QA Systems Manager, you’ll act as a key member of the Quality leadership team and take ownership of site-wide quality processes, with particular … compliance guidance and driving a strong quality culture. Key Responsibilities: Lead the development, maintenance and ongoing compliance of the site QMS in line with GxP requirements Act as site lead for data integrity, ensuring systems and processes support secure, traceable and compliant data management Oversee the validation master plan and … the site Manage and improve key quality systems including change control, CAPA, deviations, document control and training compliance Provide input and quality guidance on GxP-related investigations, audits and continuous improvement initiatives Deliver training and coaching across departments to reinforce best practice in quality and compliance Maintain oversight of system More ❯

completed contemporaneously e.g. users are provided with access when applicable, documents are reviewed and approved in a timely manner to facilitate the progression of GxP activities. All users are appropriately trained and supported when using the MasterControl Software. Documentation maintained outside of the MasterControl system is maintained in an easily … Controls, BMRs & audit/inspection actions are closed timely and in a RFT state. Job Background Minimum of 3 years experience working in a GxP environment. IT literate, experience managing and operating an electronic QMS. English language required. Why us More ❯

Data Engineer - Leading Pharmaceutical Company - Manchester (Tech Stack: Data Engineer, Databricks, Python, Power BI, AWS QuickSight, AWS, TSQL, ETL, Agile Methodologies) About the Role: We are seeking a talented and experienced Data Engineer on behalf of our client, a leading More ❯