76 to 100 of 114 GMP Jobs

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 ...

serves as the subject matter expert responsible for translating pharmaceutical microbiology laboratory processes into validated LabVantage LIMS solutions. This role combines deep knowledge of GMP microbiology testing with hands on experience configuring, validating, and supporting laboratory information management systems in regulated pharmaceutical environments. The position partners quality control, microbiology, quality … regulatory requirements into system configurations and functional specifications. Support system validation activities, including requirements documentation, testing, traceability, and qualification protocols. Ensure compliance with GMP, 21 CFR Part 11, data integrity principles, and global pharmacopoeial requirements. Collaborate with QC Microbiology, Quality Assurance, Validation, and IT teams to implement new methods ...

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 ...

validation protocols. Contribute to Lean manufacturing and Continuous Improvement activities. Collaborate with Engineering, Manufacturing, Quality and other technical teams. Ensure equipment activities comply with GMP and applicable regulatory requirements. Develop technical expertise in aseptic filling and lyophilisation systems. Qualifications & ExperienceBachelor's degree in Engineering or a related discipline, or equivalent … relevant experience. Engineering experience within biologics, pharmaceutical or regulated manufacturing. Experience working within a GMP environment. Strong equipment troubleshooting and technical problem-solving capabilities. Ability to work effectively across multidisciplinary teams. For a confidential discussion and more information on the role, please contact Kevin Griffin ...

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 ...

space - clinical trial systems, clinical data quality, and inspection readiness for sponsors and CROs - though the team also picks up broader GxP work (GMP, GDP, GLP‐adjacent systems) where a client needs it. Most clients sit in the 30-200 employee range - organisations sophisticated enough to know exactly what they … client‐facing consultancy role as opposed to purely in‐house Inspection experience with FDA, MHRA, or EMA specifically involving GCP systems Broader GxP exposure - GMP, GDP, or quality systems outside clinical trials - for consultants who want to flex across service lines Familiarity with eQMS implementation, data migration validation ...

equipment and electronic systems. Manage the procurement, validation, qualification, and deployment of new or upgraded QC equipment and systems. Ensure compliance with GMP, data integrity guidelines, and corporate standards for QC operations. Develop and maintain a long-term equipment replacement plan to meet testing requirements. Oversee new product introductions, method … systems, including their qualification and validation. Experience in managing QC equipment and systems, including acting as a laboratory administrator or end-user. Proficiency in GMP guidelines, data integrity requirements, and regulatory compliance. Excellent communication, leadership, and project management skills. Ability to analyze complex data and present findings clearly. Proficiency ...

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 ...

months, potential continuation through a multi-year program Hours: 40 hours per week Rate: $(Apply online only) all in rate Industry: Pharmaceutical/GMP Manufacturing Project: Major $4.5 billion pharmaceutical manufacturing development The Opportunity We are seeking a specialist BMS/EMS Subject Matter Expert with genuine pharmaceutical GMP experience … manufacturing development in Virginia. This is not simply a commercial building-management position. The BMS/EMS systems will operate within a validated GMP environment , making previous experience designing, specifying, implementing and commissioning BMS/EMS systems within pharmaceutical manufacturing essential. The successful candidate will take an established concept ...

monitoring and microbial identification. Collaborate with QC Microbiology, QA, Validation and IT to drive compliant methods, participate in inspections, and ensure data integrity under GMP and 21 CFR Part 11. #J-18808-Ljbffr ...

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 ...

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 ...

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 ...

solution preparation. Ensure top-tier standards by performing visual and instrumental checks on raw materials and finished goods in line with Good Manufacturing Practice (GMP). Maintain a clean, pristine workspace following 6S principles and COSHH/EHS safety guidelines. Use digital interface systems (HMI, POMS, ETMS) to log batch ...

solution preparation. Ensure top-tier standards by performing visual and instrumental checks on raw materials and finished goods in line with Good Manufacturing Practice (GMP). Maintain a clean, pristine workspace following 6S principles and COSHH/EHS safety guidelines. Use digital interface systems (HMI, POMS, ETMS) to log batch ...

visual and instrumental inspections of raw materials and finished goods. You'll play a vital role in identifying defects and maintaining Good Manufacturing Practice (GMP). Safety & Standards: Maintain a "Safety First" mindset by adhering to COSHH and EHS guidelines and keeping your workspace pristine using 6S principles. Data Integrity ...

Specialist to deliver data services to our clients, which include data and benefit audits, preparing data strategies and plans, undertaking various pension rectifications including GMP rectification and equalisation. While we continue to help clients meet their GMP objectives, the data challenges our clients face are becoming more diverse which gives ...

computer systems, processing warehouse transactions, writing professional emails, organising documentation and ensuring stock and warehouse records are accurate. Pharmaceutical experience would be preferred, especially GMP or GDP knowledge, but this is not essential. Strong SAP, ERP, warehouse administration and computer skills are the key requirements. The Role As a Warehouse … emails and communicating clearly with internal and external contacts Maintaining high levels of accuracy, organisation and traceability across warehouse documentation Working in line with GMP, GDP and pharmaceutical compliance standards where required What Were Looking For We are looking for candidates who: Have previous experience in warehouse administration, logistics, distribution ...

computer systems, processing warehouse transactions, writing professional emails, organising documentation and ensuring stock and warehouse records are accurate. Pharmaceutical experience would be preferred, especially GMP or GDP knowledge, but this is not essential. Strong SAP, ERP, warehouse administration and computer skills are the key requirements. The Role As a Warehouse … emails and communicating clearly with internal and external contacts Maintaining high levels of accuracy, organisation and traceability across warehouse documentation Working in line with GMP, GDP and pharmaceutical compliance standards where required What Were Looking For We are looking for candidates who: Have previous experience in warehouse administration, logistics, distribution ...

optimal stock levels of consumables to support the team and ensure maximum throughput and efficiency. Safety & Compliance: Uphold excellent housekeeping to Good Manufacturing Practice (GMP)/Good Laboratory Practice (GLP) standards, strictly adhering to all safety recommendations, including proper PPE usage, and contributing to safety assessments. Process Improvement: Proactively identify ...

Contract. Job Purpose The Temporary QA Document Control Associate supports the Quality Assurance (QA) department by assisting with the digitization, organization, and verification of GMP documentation. This position is responsible for scanning controlled documents and ensuring that electronic records are complete, legible, and are an accurate representation of the original … data integrity and document accuracy. Principal Accountabilities Ensure compliance with all relevant laws and regulations as well as company procedures, policies, and SOPs. Scan GMP documentation using approved/appropriate document scanning procedures. Verify that scanned electronic documents are complete, legible, and accurately represent the original paper documents and compliant ...

Eblex Group is supporting a growing biotechnology company with an expanding clinical pipeline in the search for a Director Clinical Quality Assurance with GMP exposure. This broad QA role sits within a lean biotech environment and works closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations ...