24 of 24 Permanent GxP Jobs in the UK excluding London

of scientific computing software and frameworks Previous experience in biotech or pharmaceutical industries Experience with cloud platforms (AWS, Azure) ITIL certification Security certifications (CISSP, CISM, or similar) Experience with GxP compliance Experience with pharmaceutical industry regulations Previous experience managing technical debt in regulated environments AskBio Inc . click apply for full job details More ❯

Veeva Clinical Vault as an end user, business, or system administrator Ability to effectively interface with CROs and software vendor Previous experience working in clinical trials, with emphasis on GxP and compliance Has a sound working knowledge of clinical operations, clinical processes, Trial Master File regulations medical terminology, global CROs and vendor management Excellent interpersonal and communication skills, both written More ❯

make a broad application of principles, theories, concepts, and techniques used in the applicable technical or business discipline and working knowledge of interrelated fields. Support validation of ISO/GxP regulations to ensure standards are achieved. Exercises judgment using generally defined practices and policies in selecting methods and techniques for arriving at solutions. Frequent inter-organizational and external customer contacts. More ❯

collaboration and change leadership skills Expertise in digital product lifecycle, from experimentation to scale Experience supporting regulatory audits and inspections involving emerging technologies, including AI and automation, in a GxP or highly regulated environment Our Benefits CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of More ❯

System Validation training desirable. Knowledge, 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 installations and version upgrades Data More ❯

in a leadership capacity. Strong knowledge of R&D processes, including discovery, translational, clinical development, and regulatory submissions Proven experience in enterprise data governance, architecture, and platform design in GxP environments. Familiarity with AI/ML enablement, though not focused on algorithm development. Strong stakeholder engagement, communication, and change leadership skills. Expertise with modern data stack: cloud platforms, data lakes More ❯

For: Master's degree or PhD in Life Sciences, Behavioral or Educational Sciences, with expertise in training needs assessment and curriculum development. Minimum of 5 years' experience in a GxP-regulated environment, with solid knowledge of pharmaceutical operations and production methods. Strong background in Quality systems, Operational Excellence (OpEx), TPM, and HSE systems. Demonstrated ability to think strategically and manage More ❯

a strong emphasis on stakeholder management and effective communication with senior managers and directors. What are we looking for? Experience delivering business changes or IT business system projects to GxP environment, either in a pharma site or equivalent a must have Demonstrated experience in IT Project Management. Demonstrated experience in stakeholder management and presenting to senior managers and directors. Experience More ❯

teams and external vendors Support installation/configuration of validated and non-validated systems Assist in patching, updates, and system maintenance Ensure adherence to validation standards such as CSV, GxP, and 21 CFR Part 11 Maintain accurate support records via the helpdesk system Provide onboarding and training to end users Identify and propose improvements in IT services and system performance More ❯

pharmaceutical sites would be highly advantageous. Requirements Experience working within pharma and with business stakeholders to deploy IT systems Experience managing life cycle of a MES solution in an GxP environment Knowledge blend of pharmaceutical manufacturing business, business processes and IT system components If this is of interest please apply or contact Altered Resourcing for more info. More ❯

working with open-source bioinformatics tools and APIs Comfortable building end-to-end ML pipelines in cloud environments Familiarity with regulatory considerations in clinical or research settings (e.g., HIPAA, GxP More ❯

similar domains Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings Track record of working with both custom and off-the-shelf platforms in regulated (GxP) environments - such as in manufacturing, QC or clinical settings Strong written documentation and stakeholder engagement skills Confidence working across departments and communicating with technical and non-technical audiences This is More ❯

similar domains Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings Track record of working with both custom and off-the-shelf platforms in regulated (GxP) environments - such as in manufacturing, QC or clinical settings Strong written documentation and stakeholder engagement skills Confidence working across departments and communicating with technical and non-technical audiences This is More ❯

Linux, and Android. Preferred Requirements: Server-based administration experience. Experience in a startup or rapidly changing environment. Experience working with a quality program and quality standards. Experience in a GxP environment. Experience with the following: FortiGate firewalls or similar. Ubiquity Access Points or similar. Intune MDM for Windows and MAC devices. Microsoft Active Directory/EntraID. Accounting and ERP systems. More ❯

with our AMS Partner to implement and troubleshoot end-to-end solutions, supporting a robust and scalable environment. Compliance and Regulatory Adherence: Ensure all processes adhere to industry standards, GxP regulations, FDA 21 CFR Part 11, and internal governance frameworks. Monitor system performance and integration functionalities to support audit readiness and risk mitigation. Qualifications & Experience Experience: At least 10+ years … capabilities, with a demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions. Industry Insight: Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments. Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards. Educational Background & Certifications: Bachelor's degree in Information Technology, Engineering, Business, or a related field. SAP certifications in More ❯

E-WorkBook software, IDBS has extended its flexible, scalable solutions to the IDBS Polar and PIMS cloud platforms to help scientists make smarter decisions with assured confidence in both GxP and non-GxP environments. Do you want to work in a dynamic, fast paced, high performing, safe to fail and fun environment which is founded on trust, empowerment and autonomy More ❯

clear, efficient, and well-documented LIMS configurations and scripts, following best practices and compliance standards. Participate in system reviews and validation activities to ensure system quality, regulatory compliance (e.g., GxP , 21 CFR Part 11), and data integrity. Troubleshoot, debug, and upgrade existing LIMS systems to ensure optimal laboratory operations and minimal downtime. Contribute to the full system lifecycle, from requirements … management systems. Proficient in system configuration, scripting, and integration with laboratory instruments and enterprise systems (e.g., ERP). Strong understanding of laboratory processes, data management, and regulatory requirements (e.g., GxP , 21 CFR Part 11). Experience with software development methodologies (e.g., Agile, Scrum) and system validation practices. Familiarity with database technologies (e.g., SQL) and web services (e.g., REST, SOAP). More ❯

to join our dynamic team at a leading pharmaceutical manufacturing site. About the Role As the Business Systems Manager , you will be the key IT application owner for critical GxP business systems including Tulip , EMS , SEAVision , CMMS , and more. You’ll lead the full lifecycle management of these systems, ensuring compliance, performance, and alignment with business goals. Key Responsibilities Business … System Lifecycle Management Own and manage assigned GxP systems, ensuring compliance with pharma industry standards. Oversee issue resolution, upgrades, security, vendor and license management. Deliver high-quality service using ServiceNow and build a Center of Excellence for Tulip and other platforms. Define and maintain long-term system roadmaps. Leadership & Strategic Planning Represent IT on the Operational Leadership Team (OLT) , ensuring … effectively. Team Management Lead and develop a team of System Analysts and CSV professionals , fostering growth and excellence in service delivery. What We’re Looking For Proven experience managing GxP systems in a pharmaceutical or regulated manufacturing environment. Strong understanding of IT service management, compliance, and system lifecycle. Leadership experience with cross-functional teams and external vendors. Project management skills More ❯

Pharmaceutical manufacturing environments. About the Role: As an IS Support Analyst, you'll act as a vital link between the IT Helpdesk and end users working in highly regulated GxP environments. You will troubleshoot issues, maintain system integrity, and ensure minimal downtime of business-critical and validated systems. This role is key to supporting seamless operations in both laboratory and … and specialized systems like LIMS, SCADA/HMI, and PLC-integrated devices. Collaborate with infrastructure teams and vendors to resolve escalated issues. Ensure compliance with Computer System Validation (CSV), GxP, and 21 CFR Part 11 standards. Document support activities accurately using the IT helpdesk system. Deliver technical onboarding and system usage training to end users. Proactively recommend improvements to enhance … and communication skills. Ability to prioritise tasks and manage time effectively under pressure. Desirable Experience: Previous experience working in pharmaceutical, biotech, or laboratory settings. Familiarity with validated systems and GxP environments. This is an excellent opportunity to join a collaborative, compliance-focused environment and make a meaningful impact supporting essential IT systems. If you're ready to bring your skills More ❯

E-WorkBook software, IDBS has extended its flexible, scalable solutions to the IDBS Polar and PIMS cloud platforms to help scientists make smarter decisions with assured confidence in both GxP and non-GxP environments. Do you want to work in a dynamic, fast paced, high performing, safe to fail and fun environment which is founded on trust, empowerment and autonomy … the technical implementation plan and backlog refinement. Provide technical perspective to products enhancements & new requirements activities. Optimize Spark-based workflows for performance, scalability, and data integrity, ensuring alignment with GxP and other regulatory standards. Research, and promote new technologies, design patterns, approaches, tools and methodologies that could optimise and accelerate development. Apply strong software engineering practices including version control (Git … pipelines that process clinical and pharmaceutical data efficiently, reducing data latency and improving time-to-insight for research and regulatory teams. Enabled regulatory compliance by implementing secure, auditable, and GxP-aligned data workflows with robust access controls. Improved system performance and cost-efficiency by optimizing Spark jobs and Databricks clusters, leading to measurable reductions in compute costs and processing times. More ❯

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

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

Data Engineer Join a Trailblazing Team in Clinical Research Data ManagementStep into a role that places you at the cutting edge of clinical trials, leveraging Electronic Health Record (EHR) data to revolutionise patient care and research. Based in the innovative More ❯

We provide resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing . Job Description We are seeking a Developer/Analyst to support a GXP-compliant application. Participate in the development and support of a Java application being migrated from Java 1.4 to Java 1.7. Work on various tiers of a web application, including JSPs … services, and data access. Write SQL scripts for administrative functions. Prepare application-specific documentation such as requirements, design documents, SOPs, and work instructions. Manage documents using a GXP-compliant document management system. Oversee workflow for releases through standard change management tools. Exhibit excellent verbal and written communication skills. Prioritize tasks effectively and handle multiple responsibilities. Required Technologies Proficiency in Java More ❯