76 to 100 of 150 GMP Jobs

review, user access management and continuous improvement. Develop, maintain and improve manufacturing software systems, electronic records, reporting tools and digital workflows in compliance with GMP, FDA, ISO 13485, 21 CFR Part 11 and applicable regulatory requirements. Lead Computer System Validation (CSV) activities, including the development and execution of Validation Plans … Basic SQL knowledge and ability to create database queries. Knowledge and experience with Power Bi, Power Apps, Power Automate is desired. Good knowledge of GMP/FDA regulatory requirements and current Health and Safety Regulations legislation. Proven Project Management skills through the delivery of business-critical projects. ...

Baxter Healthcare Ltd. in Thetford is seeking a Multi-skilled Automation Bias Maintenance Engineer to join the Operational Maintenance Engineering team. You will perform plant-wide reactive and proactive maintenance and support new installations across ...

join a site-based commercial team in Newcastle, supporting a major hyperscale data centre programme in North East England. The role focuses on GMP procurement, contract administration and post-contract cost control, including valuations, forecasts and final accounts, working with contractors, consultants and client representatives to ensure robust cost governance ...

delivering a major hyperscale data centre programme in North East England. You will support commercial delivery, cost control, and governance across large packages, including GMP conversions, with strong collaboration among contractors, consultants, and client representatives. This role emphasizes data-driven insights and proactive risk management. #J-18808-Ljbffr ...

Limited is seeking a skilled data engineer to design, develop and operate scalable ETL/ELT pipelines across structured and unstructured data in a GMP-like cloud environment. You will build batch and real-time processing solutions using BigQuery, Dataflow, Cloud Storage, Pub/Sub and related GCP services, while ...

improve operational efficiencies using automation and data analytics. The successful candidate will work closely with senior management to ensure digital technologies are suitable for GMP-compliant use. This position supports relocation and offers a competitive salary along with comprehensive benefits, requiring at least three days on-site each week. #J ...

Conveyor Systems and Thermal processing equipment. 3. City & Guilds 2382 (minimum of 18th Edition Regulations) 4. Familiar with the requirements of working within a GMP facility. 5. Excellent internal and external communications skills 6. Experience of working an on-call maintenance system. TPBN1_UKTJ ...

Conveyor Systems and Thermal processing equipment. 3. City & Guilds 2382 (minimum of 18th Edition Regulations) 4. Familiar with the requirements of working within a GMP facility. 5. Excellent internal and external communications skills 6. Experience of working an on-call maintenance system. ...

Responsibilities: Under general direction, provides support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs) Participates in project teams to provide review and approval of project Validationdocumentation according to applicable approval matrix ...

Sanofi's Digital Lighthouse ambitions. You will work across a broad technology stack including PLCs, SCADA, MES, Historian, and IIoT platforms, operating within a GMP-regulated environment where patient safety and product quality are paramount. Ready to get started? Join a global network that powers how Sanofi delivers - seamlessly, purposefully … inspection-ready for regulatory audits (FDA, EMA, HPRA) Manage change control, deviation investigations, and CAPAs related to automation systems in compliance with site GMP procedures Support the site's Business Quality Representative (BQR) process for GxP digital solutions Data & Digital Leverage OSIsoft PI and Ignition platforms to develop dashboards, reports ...

product quality to ensure customer specifications and quality requirements are consistently achieved. Maintain and continuously improve food safety and quality management systems, including HACCP, GMP, and customer-specific standards. Ensure compliance with all food safety, legal, regulatory, and customer requirements. Auditing & Traceability Plan, conduct, and close out internal audits. Maintain … performance. Monitor quality KPIs and drive initiatives that enhance product quality, reduce waste, and improve efficiency. Essential Strong knowledge of food safety systems, HACCP, GMP, quality standards, and audit requirements. Demonstrated experience managing traceability systems and conducting traceback investigations. Strong analytical, problem-solving, and root cause investigation skills. Excellent attention ...

issues and opportunities for improvement. Calibration: Take responsibility for the calibration and control of quality equipment, ensuring records are accurate and up to date. GMP Auditing: Conduct and coordinate GMP audits, ensuring standards are maintained and actions are followed through. Internal Audits: Assist with internal audits and support the site … ideally have: Previous experience working in a QA/Quality role, preferably within food manufacturing, FMCG or fresh produce A good understanding of GMP, HACCP, food safety and quality systems. Experience with non-conformance, CAPA and Root Cause Analysis. Experience supporting or completing audits. Strong attention to detail and excellent ...

transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing the EU and FDA GMP requirements. Job Description Major Activities To support the development and validation of established and novel analytical test methods for the current and newly developed gene … support of the method transfer and validation activities performed ensuring compliance requirements are maintained. Ensure all methods are validated and transferred to QC GMP labs in compliance with regulatory standards and adhere to data integrity requirements. Generate method SOPs are developed and implemented to support all validated methods. Ensure these ...

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. … have the right to work in this location or hold an EU passport. Responsibilities Implement and maintain IT systems and processes in line with GMP regulations, focusing on Quality Systems (e.g., LIMS, CDS, QC equipment applications). Provide day‐to‐day IT support, including issue resolution, system changes, and service ...

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 ...

Oversee swabbing and sampling programmes, ensuring all activities are completed on time and any out-of-specification results are addressed. Lead the site's GMP audit programme and support customer and third-party audits. Ensure completion of actions arising from internal and external audits. Promote a culture of continuous improvement … Quality Assurance or Technical role within the food manufacturing industry. Experience conducting internal audits. Strong knowledge of food safety, quality systems, and GMP standards. Excellent communication and stakeholder management skills. The ability to make informed decisions quickly in relation to food safety, legality, and quality. Strong organisational skills ...

milestone. Completing, reviewing and approving quality related documentation including but not limited to validation documents, change controls, deviations and risk assessments in accordance with GMP and standard operating procedures. Preparing, reviewing, approving and executing of CSV documentation (e.g. plans, protocols, reports, periodic reviews) Contributing to the set up and execution … required. Providing subject matter expertise to all areas of the business, particularly in audits. About You Proven experience in Computer System Validation within a GMP regulated environment. A background in supervising, influencing or leading teams. Exceptional attention to detail, with a determination to continually develop and improve standards. Demonstrable experience ...

closure • Monitoring and improving KPI performance, supporting investigations and audits • Participating in internal, customer and group technical audits to ensure compliance with QMS, GMP and HACCP • Identifying and escalating non-conformances, recommending improvements and reducing recurring issues • Managing supplier interactions, ensuring non-conformances are addressed and root causes resolved • Investigating … looking for • Strong knowledge of food safety, quality systems and raw material assurance within a manufacturing environment • Confidence conducting audits and applying QMS, GMP and HACCP requirements • Ability to assess raw materials and packaging against specifications with a high level of accuracy • Experience managing supplier non-conformances and supporting root ...

milestone. Completing, reviewing and approving quality related documentation including but not limited to validation documents, change controls, deviations and risk assessments in accordance with GMP and standard operating procedures. Preparing, reviewing, approving and executing of CSV documentation (e.g. plans, protocols, reports, periodic reviews) Contributing to the set up and execution … required. Providing subject matter expertise to all areas of the business, particularly in audits. About you Proven experience in Computer System Validation within a GMP regulated environment. A background in supervising, influencing or leading teams. Exceptional attention to detail, with a determination to continually develop and improve standards. Demonstrable experience ...

Multi-Skilled Engineer, you will play a key role in maintaining site equipment, ensuring production efficiency and upholding high standards of food safety, GMP and Health & Safety. Key responsibilities include: Championing and maintaining Good Manufacturing Practice (GMP) standards across the site Fault finding and troubleshooting across electrical, mechanical and control ...

deliver efficient, scalable solutions. Key Responsibilities: Lead process improvement and automation initiatives Develop and implement technical solutions for manufacturing challenges Ensure compliance with GMP and other regulatory requirements Utilise ERP systems for planning and reporting Collaborate with cross-functional teams to deliver projects on time and within scope About … experience in high-end manufacturing environments such as pharma, electronics, or cleanroom operations. Knowledge of automation systems and ERP platforms is essential, and GMP experience is highly desirable. You will ideally have: Degree in Engineering or related discipline Proven experience in Lead Process Engineering and automation ERP system proficiency Understanding ...

must be eligible Job Purpose The Salesforce Application & Analytics Manager will be responsible for the strategic management, support, development, and continuous improvement of the GMP Application and associated analytics capabilities. The role will ensure the effective operation of the Salesforce platform, delivery of the application roadmap, and development of high … driving innovation and data-driven decision-making. Key Responsibilities Salesforce Application Management Own the day-to-day administration, maintenance, support, and enhancement of the GMP Application hosted on the Salesforce platform. Act as the primary subject matter expert for the application, ensuring stability, performance, and user satisfaction. Develop and maintain ...

responsible for the raw material/Finished Product and packaging components booking in sampling and testing process. To test and report results to GMP standards as per company SOP's. To perform routine physical testing as per approved methods. To calibrate and maintain equipment in the laboratories. To troubleshoot routine … laboratory issues when they arise. To operate standard laboratory instruments including HPLC, GC, Auto titrator, UV spectrometer and Dissolution apparatus. To maintain laboratories to GMP standards. To routinely test raw materials, finished product, stability samples and investigational samples using analytical techniques. Sample booking in and collection for routine analysis. Managing ...

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 ...

programme and support regulatory inspections Approve suppliers and starting materials using a risk-based approach Prepare, approve and distribute SOPs, policies and other master GMP documents Arrange export certificates and traceability for products of animal origin What you'll need to apply for the QA Officer A bachelor's degree … scientific or technical discipline Experience in a Quality role within a pharmaceutical or food environment Working knowledge of quality management systems and GMP Interested? Click Apply to find out more, or call the office to discuss. If you click ' Apply ', we may contact you via email, phone & text message regarding ...