51 to 75 of 75 GMP Jobs

support the achievement of Grade AA BRCGS status. You'll manage non-conformances, customer complaints and corrective actions, drive improvements in good manufacturing practice (GMP), and work closely with production, technical and development teams to embed a strong quality culture. This is an excellent opportunity to influence manufacturing standards, develop ...

technology strategy across manufacturing, laboratories, quality, engineering, warehouse operations, automation, infrastructure, data, cybersecurity, and enterprise platforms. Working at the heart of a highly regulated GMP environment, you will ensure technology investments support operational excellence, product quality, regulatory compliance, patient safety, and long-term digital transformation objectives. This is a highly … digital manufacturing initiatives including MES, electronic batch records, paperless production, laboratory digitisation, analytics, AI, integration, cloud, and edge technologies. Ensure architecture decisions align with GMP, GxP, CSV/CSA, data integrity, cybersecurity, validation, and operational resilience requirements. Develop and maintain architecture artefacts including capability maps, data flows, system landscapes, integration ...

standards. Working closely with cross-functional teams, you'll oversee key quality activities, support continuous improvement initiatives, and play a vital role in maintaining GMP compliance across the site. Key responsibilities include: Lead and support the QA team, providing coaching, training and day-to-day guidance. Ensure quality activities … completed in line with GMP, compliance and business requirements. Review batch documentation and support product release activities. Oversee investigations, deviations, CAPAs and change controls, ensuring issues are resolved effectively. Monitor quality performance and drive continuous improvement initiatives. Manage customer and product quality complaints, ensuring thorough investigation and resolution. Deliver ...

Provide technical support, troubleshooting, and ongoing maintenance for QC laboratory electronic systems. Manage and maintain master data to ensure system performance remains compliant with GMP and data integrity requirements. Support system enhancements, software updates, new module deployments, and change control activities. Assist with the qualification, validation, and implementation … this role, you will possess: A degree in a scientific discipline, or equivalent industry experience. Proven experience supporting laboratory electronic systems within a pharmaceutical GMP environment. Strong working knowledge of LIMS and/or CDS platforms, including master data management. Excellent communication skills with the ability to explain technical concepts ...

scale-up and technology transfer activities Leading technical investigations and troubleshooting manufacturing processes Driving process optimisation and continuous improvement projects Supporting validation activities and GMP documentation Working closely with Production, QA, Product Development and Engineering teams Assisting with new equipment evaluation and implementation Providing technical expertise to support business-critical … project management skills Experience with MSAT, process validation, technical transfer or product lifecycle management Ability to work across multiple projects and stakeholders Knowledge of GMP and pharmaceutical manufacturing environments Experience with solid dose products would be a distinct advantage. What we offer Average 36-hour working week (with ...

Specialist will play a key role in supporting site validation activities across a range of projects. This is a great opportunity for someone with GMP validation experience looking to build on their existing knowledge within a supportive and expanding team. Candidates with equipment or process validation experience from pharmaceutical … other GMP-regulated manufacturing environments are encouraged to apply. The role: Plan and execute validation activities in line with site validation plans and project timelines. Author and maintain validation protocols and reports across multiple validation areas such as: Cleaning validation Computerised systems validation Equipment and utilities qualification Process validation Interpret ...

Provide technical support, troubleshooting, and ongoing maintenance for QC laboratory electronic systems. Manage and maintain master data to ensure system performance remains compliant with GMP and data integrity requirements. Support system enhancements, software updates, new module deployments, and change control activities. Assist with the qualification, validation, and implementation … this role, you will possess: A degree in a scientific discipline, or equivalent industry experience. Proven experience supporting laboratory electronic systems within a pharmaceutical GMP environment. Strong working knowledge of LIMS and/or CDS platforms, including master data management. Excellent communication skills with the ability to explain technical concepts ...

candidate will bring strong experience with MES platforms and integrated manufacturing systems, with particular expertise in PAS-X, DeltaV, and SAP within a regulated GMP environment. Description: Serve as the MES Subject Matter Expert supporting manufacturing operations and digital manufacturing initiatives. Provide technical leadership for MES configuration, implementation, optimization, troubleshooting … changes, upgrades, testing, commissioning, qualification, and validation activities. Troubleshoot complex MES and system-integration issues and drive root-cause resolution. Ensure solutions comply with GMP, data integrity, computerized system validation, and applicable regulatory requirements. Develop and maintain technical documentation, procedures, specifications, and system lifecycle documentation. Provide technical guidance and mentorship ...

trends and equipment issues, supporting CAPA activities. Assist with installation, commissioning, qualification and validation activities, including IQ/OQ/PQ. Ensure compliance with GMP, GxP and ALCOA+ data integrity requirements. Analyse data from serialisation, automation and production systems to identify opportunities for performance improvement. Support and maintain PLCs, HMIs … related discipline Experience supporting serialisation, automation or packaging line systems within a manufacturing environment. Strong fault‐finding and troubleshooting capabilities Experience working within GMP, pharmaceutical, medical device or other highly regulated environments. Understanding of packaging machinery, automation systems and data integrity requirements. Working knowledge of PLCs, HMIs, vision systems, scanners ...

architectures supporting business- critical production systems. Develop target-state architectures and migration strategies for large-scale technology modernisation initiatives. Ensure solutions comply with GMP/GxP requirements, validation standards, cybersecurity frameworks, and industry best practices. Experience required Extensive experience as a Solutions Architect, Enterprise Architect, or Technical Architect within regulated … environments, including industrial systems, plant infrastructure, and manufacturing technology. Proven experience delivering complex IT infrastructure transformation and migration programmes. Significant cybersecurity experience within GMP/GxP-regulated environments. #J-18808-Ljbffr ...

role requires hands-on technical leadership across design, commissioning, validation, and continuous improvement, collaborating with Quality, Validation, and Digital teams in a fast-paced GMP environment. #J-18808-Ljbffr ...

Biomedical/Electronic Engineer to support test processes and manufacturing design at our UK site. The role requires developing documentation, validating processes, and ensuring GMP compliance with cross-functional collaboration and external vendors. The position emphasizes analytical problem solving, effective communication, and training manufacturing teams. It offers on-site work ...

leading life sciences manufacturing organization in the UK. You will lead MES configuration, integration, and lifecycle activities across PAS-X, DeltaV and SAP within GMP environments. Collaborating with Manufacturing, Automation, Engineering, Quality, IT/OT and Validation, you will ensure reliable system performance, data integrity, and audit readiness while guiding ...

Proclinical seeks a Senior QC Systems Technical Specialist to support laboratory electronic systems (LIMS and CDS) within a GMP-regulated QC environment. You will manage master data, assist with validation activities, and maintain qualification documentation to ensure data integrity and regulatory compliance. In this role you will collaborate with ...

critical production systems. The role is remote with an initial 6-month contract for a high-impact life sciences programme, requiring extensive experience in GMP/GxP and cybersecurity within #J-18808-Ljbffr ...

function, support and develop the QA team, and make sure products meet customer, legal and internal quality standards. You'll also be involved in GMP, audits, quality control, continuous improvement and working closely with Production to resolve quality issues. As QA Team Leader, you'll work closely with the Operational … quality concerns are identified and reported promptly. Carry out additional quality assessments, including dry matter and hot box testing, where required. Manage the site GMP audit system and participate in internal auditing activities. Support preparation for internal and external audits. Assist with recording and monitoring weekly quality KPIs. Support ...

Sharp Services, LLC seeks a Computerised Systems Validation Specialist to oversee CSV status of GMP IT systems at the Rhymney site, with onsite or hybrid working and travel to European sites. You will maintain validation master plans, prepare documentation, and coordinate validation activities with IT, Operations, Supply Chain and QA. … role requires GMP knowledge, experience in pharma environments, and the ability to travel regularly to Sharp sites in Belgium and the Netherlands. #J-18808-Ljbffr ...

dedicated Quality Analyst to support the digital transformation journey of a manufacturing site, focusing on implementing and maintaining IT systems that align with GMP regulations. This role will primarily involve working with Quality Systems such as LIMS, CDS, and other QC equipment applications, while also supporting broader manufacturing IT needs. ...

research use. We're seeking an Embedded Software Engineer to help develop, maintain, and extend our software, which controls our instruments and supports GMP‐compliant workflows. You'll be joining at a pivotal stage for the company, contributing to the ongoing development of the GMP instrument software, playing a role … instrument software and in‐house manufacturing rigs Collaborate with engineers and scientists to refine requirements, solve technical challenges, and implement effective solutions Contribute to GMP‐compliant software development, including clear documentation, testing, and certifications Write robust, maintainable, and well‐tested code in line with internal standards, participating in design reviews ...

research use. We're seeking an Embedded Software Engineer to help develop, maintain, and extend our software, which controls our instruments and supports GMP-compliant workflows. You'll be joining at a pivotal stage for the company, contributing to the ongoing development of the GMP instrument software, playing a role … instrument software and in-house manufacturing rigs Collaborate with engineers and scientists to refine requirements, solve technical challenges, and implement effective solutions Contribute to GMP-compliant software development, including clear documentation, testing, and certifications Write robust, maintainable, and well-tested code in line with internal standards, participating in design reviews ...

research use. We're seeking an Embedded Software Engineer to help develop, maintain, and extend our software, which controls our instruments and supports GMP-compliant workflows. You'll be joining at a pivotal stage for the company, contributing to the ongoing development of the GMP instrument software, playing a role … instrument software and in-house manufacturing rigs Collaborate with engineers and scientists to refine requirements, solve technical challenges, and implement effective solutions Contribute to GMP-compliant software development, including clear documentation, testing, and certifications Write robust, maintainable, and well-tested code in line with internal standards, participating in design reviews ...

STEMCELL Technologies UK Ltd. seeks an Embedded Software Engineer to develop, maintain, and extend software controlling instruments and supporting GMP workflows. You will contribute to GMP-compliant software development and participate in design reviews with a multidisciplinary team. The role is ideal for an early-career engineer or post ...

STEMCELL Technologies Inc. is seeking an Embedded Software Engineer in Cambridge to develop and maintain software for our GMP-compliant instruments and in-house manufacturing rigs. You will collaborate with engineers and scientists to refine requirements, implement robust features, and ensure documentation and testing meet internal standards. The role supports ...

/4HANA PP/QM consultant for the pharmaceutical sector in the United Kingdom. You will lead end-to-end implementations, ensuring GMP compliance and robust serialization/Track & Trace capabilities. The role focuses on PP/DS and EWM/WM, optimizing production and warehouse processes, validating MRP configurations ...

Pearl Control Systems Limited in the UK is seeking a Senior Control Systems Engineer to design, program and maintain advanced control systems for production facilities. You will help automate processes, troubleshoot issues and enhance operational ...