26 to 50 of 151 GMP Jobs

Oriented Programming Git version control Basic electrical, mechanical and pneumatic knowledge Robotics Machine Vision SCADA/MES systems Pharmaceutical or regulated manufacturing environments GAMP, GMP, 21 CFR Part 11 or EU Annex 11 Industrial communication protocols including EtherCAT, Profinet, CAN, Ethernet/IP and Serial communications .NET ...

62443Experience with industrial automation systems and OT architecture, including integration with IT systemsFamiliarity with regulated environments and standards such as GxP (including GMP and GAMP5) and IEC 61508/61511Understanding of cyber security risk assessments, controls, and system documentationExperience in system lifecycle management, including validation, change control, and documentation practicesKnowledge ...

Growth of strategic regional chain and distributor partnerships. Forecast accuracy and reporting compliance. CRM utilization and pipeline management effectiveness. Customer retention and satisfaction. Safety, GMP, Food Safety, and Quality compliance. BRC compliance adherence. Effective management of pricing and margin objectives. Successful execution of strategic growth initiatives. EXPERIENCE AND SKILL REQUIREMENTS ...

responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical oversight of electronic systems, manages validation activities, assesses system … validated state. Identify and close existing CSV gaps to ensure compliance with Annex 11 and data integrity requirements. EudraLex Volume 4 Good Manufacturing Practice (GMP) guidelines, laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/ ...

control. Produce weekly stock expenditure reports highlighting asset management costs and repeat product failures. Promote and support continuous improvement initiatives such as 5S, GMP, and TPM pillars. Demonstrate safe working behaviors and conform to site safety standards and procedures. Identify personal skills gaps and contribute to training and development plans. ...

manufacturing experience are unlikely to be suitable for this position. Experience with Siemens S5/S7 PLCs, inverter drives, COMPEX, hazardous areas, pneumatics or GMP environments would be beneficial, but not essential. The role You will respond to production breakdowns, carry out planned maintenance, support equipment modifications and small projects ...

system. Participate in daily maintenance meetings and continuous improvement initiatives. Assist with root cause analysis and equipment reliability projects. Maintain high standards of housekeeping, GMP and health & safety compliance. Ensure equipment is operating safely and efficiently to minimise downtime. Experience/Skills/Knowledge/Qualifications: Strong electrical maintenance background ...

improvement initiatives, including automation developments and SMED projects. Maintain accurate maintenance records and documentation. Ensure all work is completed in accordance with Health & Safety, GMP, quality and environmental standards. Support colleagues through knowledge sharing and contribute to maintaining high engineering standards across the site. About You To be successful ...

YouTube, TikTok, etc) Demonstrate advanced knowledge in Ad Serving: Campaign Manager (CM360) is a must Good understanding of GA360 and other products of the GMP suite Good understanding of Measurement Frameworks, MMM partners, Incrementality Testing, A/B Testing Experience working with industry-leading Paid Media Partners Experience managing large ...

environment Desirable 1. Experience with catheter-based or similarly complex diagnostic/therapeutic devices 2. Experience managing US FDA regulatory interactions or GLP/GMP study programmes 3. Prior experience in a Series A-B medical device company What's on Offer A pivotal, high-impact role in a well ...

coach, develop and inspire technical teams. Desirable Experience within medical devices, healthcare technology or other safety-critical industries. Knowledge of IEC 62304, ISO 13485, GMP and FDA-regulated environments. Experience with cloud platforms such as Azure, AWS or GCP. Understanding of cybersecurity for connected devices and IoT systems. Exposure ...

analytics, CRO, A/B testing, and site optimisation. Awareness of DCO platforms (Flashtalking, Sizmek, Jivox, RevJet). Understanding of attribution solutions (GMP, Neustar, Visual IQ, etc.). Experience working within regulated industries (pharma experience advantageous). Additional Information Zenith International has fantastic benefits on offer ...

MedPharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance. You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support ...

electrical schematics and technical drawings Good understanding of mechanical systems (gearboxes, bearings, conveyors, pneumatics) Knowledge of food safety standards such as BRC, HACCP, or GMP Strong problem-solving skills and ability to work independently Benefits Opportunity to work in a modern food manufacturing facility Ongoing training and development Pension scheme ...

will have experience in raw materials, technical or quality roles within food manufacturing. Bringing a strong understanding of food safety, legality, allergens, HACCP, GMP and customer codes. Being confident working with technical systems, specifications and supplier documents. You will have good analytical skills and the ability to spot risks early. ...

. Experience with process control and automated systems for production lines. Familiarilty with PID tuning for production lines. Familiarity with industry-specific regulations (HACCP, GMP, etc.) and food safety standards. Knowledge of instrumentation and process equipment . Knowledge of Java, Python, C++ and VB Scripting Familiarity with Flow Charts ...

Catalent Swindon site seeks an Associate Director, QMS & Compliance to lead the Quality Management System and regulatory affairs, ensuring GMP/FDA/MHRA compliance and continuous improvement at a leading biologics/pharmaceutical operations hub in Swindon, UK. You will develop high-performing teams, manage QMS budgets, and partner ...

backup/restore, or diagnostics standards for complex software-enabled products.Experience working in regulated or validated environments, including exposure to SAT, IQ/OQ, GMP, or automation validation practices.Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether ...

/restore, or diagnostics standards for complex software-enabled products. Experience working in regulated or validated environments, including exposure to SAT, IQ/OQ, GMP, or automation validation practices. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether ...

Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands‐on expertise with a pragmatic, client‐focused consulting approach.What … clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10).Authoring, reviewing and maintaining quality policies, standards, SOPs ...

Management System (QMS) design, transformation and implementation.In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands‐on expertise with a pragmatic, client‐focused consulting approach.What … clinical and distribution environments.Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10).Authoring, reviewing and maintaining quality policies, standards, SOPs ...

seeking a GxP IT Systems Engineer to support manufacturing operations at their Harwell site in the UK. This role involves ensuring compliance with GMP standards, providing IT support, and maintaining system integrity. The ideal candidate will have a Bachelor’s degree in a computer-related field and 3-5 years ...

PCI Pharma Services is seeking a Lead Maintenance Engineer to head the on-site Maintenance Engineering function. You will drive compliance, reliability, safety, and continuous improvement across site operations, managing budgets, assets, and regulatory requirements ...

within a QA, Quality Assurance, or Quality Control role. Experience within the food manufacturing industry is essential. Good understanding of HACCP, Food Safety, and GMP standards. Strong attention to detail and excellent record-keeping skills. Confident communication skills and ability to work collaboratively. Ability to work independently and make informed ...

sensors, relays and control systems. Complete maintenance records using SAP/CMMS. Support continuous improvement and reliability projects. Ensure all work is completed to GMP, food safety and health & safety standards. Requirements Time-served Electrical Engineer or equivalent qualification. Strong electrical fault-finding experience in a manufacturing environment. PLC troubleshooting ...