76 to 100 of 137 Permanent GMP Jobs

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 ...

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 ...

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 ...

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 ...

within the relevant area of responsibility, to control, reduce and eliminate waste within anything that we do. Adhere to high levels of GMP (Good Manufacturing Practice) and ensure 5S is carried out at all times. Any additional role-specific H&S responsibilities. Any additional role-specific Environmental responsibilities. Knowledge & Experience ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

Monitoring equipment and facilities to ensure they remain compliant and operational Managing spare parts and consumable stock levels Producing clear, accurate documentation that supports GMP and UKAS requirements Contributing ideas that improve processes, efficiency and reliability This role supports activities across both our Oak Tree House and Coleby House sites … full UK driving licence Bonus Points If You Have Experience With Chromatography systems Mass spectrometry instrumentation Chromatography Data Systems (CDS) Equipment validation and qualification GMP, UKAS or ISO 17025 regulated environments Why Join Us This is an ideal opportunity for someone early in their technical career who enjoys taking things ...

minimum of 6 months post qualification Pharmacy experience, with a minimum of 3 month Hospital Pharmacy Technical services experience Knowledge of Good manufacturing practice (GMP) and ability to apply this knowledge in practice Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order ...

Vifor is seeking a Quality Systems professional to support GMP-compliant quality systems across validation, calibration and document management. You will contribute to internal audits and continuous improvement programs while ensuring alignment with FDA/EMA requirements. The role involves collaboration with project teams and serving as a subject matter ...

workload and training of staff. You will ensure that staff undertake activities following departmental operating procedures and work in accordance with Good Manufacturing Practice, Good Clinical Practice and Good Distribution Practice. We welcome applications from Pharmacy Technicians and other Scientists such as Pharmaceutical Scientists eligible for membership registration with … running of the service; maintaining equipment according to procedures and actively encouraging adherence to all procedures relating to the aseptic services department and GMP; quality assurance activities. See attached Job Description for detailed job duties. About us Lincoln Hospital is a thriving university city and with the opening ...

Engineering Maintenance Department. Use and develop skills to allocate resources effectively for maintenance tasks Review completed work orders and service reports for GMP compliance, and provide data to address recurring downtime issues. Generate daily SCADA reports and manage the archiving of GMP documentation. Assist in developing and managing ...

Engineering Maintenance Department. Use and develop skills to allocate resources effectively for maintenance tasks Review completed work orders and service reports for GMP compliance, and provide data to address recurring downtime issues. Generate daily SCADA reports and manage the archiving of GMP documentation. Assist in developing and managing ...