26 to 50 of 76 GMP Jobs

operational teams. Desirable Experience Emerson Syncade platform administration or technical configuration. Pharmaceutical or biotechnology manufacturing environments. MES infrastructure, application deployment and system integration. GMP/GxP-regulated systems. Why Consider This Opportunity? Initial 24-month contract offering long-term project continuity. Opportunity to contribute to a major pharmaceutical manufacturing technology ...

related field 3+ years experience in Control Systems Engineering Hands on experience with DCS systems (ideally Siemens SIMATIC PCS7) Previous work experience in a GMP manufacturing environment (Pharmaceutical experience is desireable) Knowledge of GAMP frameworks Willing to work on customer sites across the Northwest Code: INDENM If you are interested ...

occasional London meetings, delivering findings for client reports. The role requires deep experience in computerised system validation, GAMP 5, 21 CFR Part 11, EU GMP Annex 11 and CDISC standards, with the ability to produce clear, actionable fixes for potential deal-impacting issues. #J-18808-Ljbffr ...

users and technically specialist R&D teams Experience with regulatory software requirements in analytical instrument markets: 21 CFR Part 11, GAAMP, GLP/GMP compliance, or equivalent Familiarity with laboratory informatics ecosystem: LIMS, ELN, data management platforms, and connectivity standards (OPC-UA, SiLA2, AnIML) Experience managing software beta programmes ...

manufacturing systems across ERP/MES and related databases. You will validate, validate, and continuously improve digital solutions that support medical device manufacturing in GMP and regulatory contexts. You will lead CSV activities, support SAP Business One processes, develop SQL queries and dashboards, and collaborate with Operations, Quality and IT. ...

Moderna is seeking an onsite Automation Engineer to lead packaging automation and DS manufacturing support at our Harwell facility. You will troubleshoot DeltaV, Allen-Bradley PLCs, HMIs, instrumentation, and networks while driving continuous improvement across ...

equipment utilizing CMMS system(SAP). MaintainsequipmentpartsandsuppliesinventoriesthroughaccuratewithdrawalfromstockutilizingSAP. Occasionally required to operate equipment such as scissor lift, man lift and forklift. Follow Good Manufacturing Procedures(GMP), perform tasks per the Master Sanitation Schedule(MSS)and follow general housekeeping guidelines and rules for Food Safety Regulations. Keep area updated with 5S. This ...

shift: 10:30 pm to 7 am Position: Full-time Pay rate: $25/hr Responsibilities Operates and maintains all equipment following SOPs, and GMP and follows all safety procedures (PPE, emergency stops, guarding, and lockouts), and ensures complete documentation and administration reports, including updating the computerized production tracking system. ...

basis of our work. Our commitment to quality ensures a safe working environment and reliable therapeutic products by adhering to the highest standards (e.g. GMP/ISO). Solidarity We always work with passion and the support of a reliable team. We value strong human relationships and a community based ...

regulated environment. You will lead technical activities across serialisation, diagnostics, data integrity and validation support, contributing to compliant, efficient manufacturing operations. Prior experience in GMP-like settings is highly desirable. #J-18808-Ljbffr ...

Technologies, Inc. in Cambridge is seeking an Embedded Software Engineer to develop, maintain, and extend instrument software and in-house manufacturing rigs, contributing to GMP-compliant workflows. You will collaborate with engineers and scientists to refine requirements, solve technical challenges, and implement effective solutions, while ensuring robust testing and clear ...

external partners to ensure robust CSV, regulatory compliance and system architecture. The role involves leading validation, lifecycle activities and audit support to align with GMP/ISO standards and business needs on a global scale. #J-18808-Ljbffr ...

United Kingdom seeks a Computer System Validation (CSV) Specialist to govern validation of GxP‐relevant computerised systems on site, ensuring compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, and GAMP5 principles. The role provides technical oversight of electronic systems, manages validation activities, and closes CSV compliance gaps ...

governance strategy and roadmap.Organisational Agility: Experience navigating large matrix organisations and leading cross-business initiatives.Regulatory Expertise: Deep knowledge of GAMP5, CSV, CSA, GDP, GMP, ISO 9001, and healthcare regulations.Process & Governance Design: Ability to build frameworks, governance standards, and risk-based decision models.Risk Management:Strong grasp of risk-based validation principles ...

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. ...

adoption. Existing Client Growth and Expansion Drive upsell and cross‐sell revenue across our existing reseller client base, expanding adoption of the Google stack (GMP, DV360, GA, GTM). Collaborate with Account Management and Martech teams to commercialise proprietary Jellyfish solutions, including Share of Model, into client growth strategies. Commercial ...

Ekco seeks an experienced Technical Architect to lead end-to-end architecture for a major enterprise device migration and workplace transformation programme within a GMP-regulated environment. The role oversees infrastructure, identity, networking, and security across multiple workstreams, ensuring scalable, secure solutions aligned to enterprise standards. The candidate will provide ...

pharmaceutical, medical device or drug manufacturing company 2+ years in Quality Assurance in a pharmaceutical, medical device or drug manufacturing company Strong GMP knowledge and in depth understanding of ICH and FDA regulations Thorough understanding of problem-solving and quality improvement tools and techniques Ability to work effectively and collaboratively ...

will play a senior, hands-on role within the Quality Assurance team. You will lead compliance with BS EN ISO 22716 Cosmetics Good Manufacturing Practice, Quality Management Systems (QMS), and company standards, working closely with SHE, QC, Production, Process R&D, and Engineering. From raw material to finished product release … approve master records, specifications, and controlled documentation (SOPs, work instructions, policies). Compliance & Standards: Maintain site compliance with BS EN ISO 22716 Cosmetics GMP and QMS standards. Act as a site Subject Matter Expert for QMS processes. QMS Management & Troubleshooting: Lead investigations into deviations, non-conformances, and customer complaints using ...

qualification, validation, and system release activities. Identify potential risks, resolve challenges, and manage changing priorities within a complex manufacturing environment. Ensure projects comply with GMP, quality, cybersecurity, validation, and data integrity requirements. Support change management activities, including the introduction of new technologies, employee training, and operational readiness. Communicate project progress … digital transformation projects. Previous experience working within the pharmaceutical or biopharmaceutical industry, preferably in a large and complex manufacturing organization. Strong knowledge of GMP requirements and experience managing projects within a GMP-regulated environment. Experience managing complex technical projects from planning and design through implementation, validation, and operational handover. Experience ...

Accord Healthcare Europe is seeking an instrumentation/calibration technician to ensure calibration systems operate reliably in a GMP environment. You will troubleshoot, calibrate, and repair equipment, using controllers, sensors and test instruments, while following drawings and specifications to diagnose faults. The role requires ONC level or equivalent in Electrical ...

PLCs. You will oversee repairs, support high-speed lines, and work with hydraulics, pneumatics, and electrical systems to ensure continuous production. The role emphasizes GMP compliance, 5S housekeeping, and proactive maintenance through SAP/CMMS platforms. #J-18808-Ljbffr ...

preventative maintenance for the R&D Pilot Line, maximise equipment availability, and support new equipment installation and qualification. You'll drive improvements, maintain GMP-compliant service records, contribute to cross-functional projects, and provide training to team members while ensuring safety and reliability. #J-18808-Ljbffr ...

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 ...

direct line team of 11 the role holder willlead operational teams on the review, selection and deployment of digital technologies, ensuring suitability for GMP complaint use. You will be based in Scotland with 3 days a week minimum on site. Relocation is supported.The role offers a competitive salary and comprehensive ...