9 of 9 Contract GMP Jobs in the UK

problem-solving skills. Good IT skills, including Microsoft Office and MRP/ERP systems. Desirable 5+ years' mechanical inspection experience. Knowledge of FDA, GMP and ISO 13485 standards. Engineering qualification, apprenticeship, or equivalent industry experience. Experience working within regulated manufacturing environments. Key Skills CMM Programming & Inspection (Essential) LK & Mitutoyo CMMs ...

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 ...

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 analyti click apply for full job details ...

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 ...

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 ...

Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems. Duties … required turnaround times. Analysing and interpreting company and client documentation to determine correct data setup. Applying established data standards, guidelines, and SOPs in a GMP setting. This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent ...

Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems. Duties … required turnaround times. Analysing and interpreting company and client documentation to determine correct data setup. Applying established data standards, guidelines, and SOPs in a GMP setting. This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent ...

Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems. Duties … required turnaround times. Analysing and interpreting company and client documentation to determine correct data setup. Applying established data standards, guidelines, and SOPs in a GMP setting. This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent ...