16 of 16 Remote GMP Jobs in the UK excluding London

as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required to client sites. What We Offer: Competitive More ❯

Education & Qualifications A Masters/B achelor's degree in business , information technology, or a related field. Advanced degrees or certifications are a plus. Itil 4 , Prince 2 or GMP is a plus Travel Requirements Position will involve up to 25% travel , mostly within Europe , Asia Pacific, and Americas. Most trips will include overnight travel . Languages English Portuguese or More ❯

for urgent issues. Education & Qualifications Bachelor's or Master's degree in Engineering, Software Development, Information Technology, or related fields. Certifications are a plus. Additional certifications like ITIL 4, GMP, or Database technologies are advantageous. Travel & Languages Travel up to 10% within Europe, Asia Pacific, and the Americas, including overnight stays. Languages: English required; Portuguese or Spanish is a plus. More ❯

Education & Qualifications A B achelor's/Masters degree in Engineering , Software development, I nformation technology, or a related field. Advanced degrees or certifications are a plus. Itil 4 , GMP or Database technologies i s a plus Travel Requirements Position involve travel up to 10 % of the time, mostly within Europe , Asia Pacific, and Americas. Most trips will include overnight More ❯

looking for professionals with these required skills to achieve our goals: Degree level qualification (or strong equivalent experience) in an appropriate scientific, technical or engineering discipline. Thorough knowledge of GMP and Regulatory requirementsin a pharmaceutical environment. Thorough operational knowledge of manufacturing unit operations and plant/laboratory equipment Ability to communicate and influence effectively at all levels of the organisation More ❯

ISA 95/88 Good understanding of industry stands communication protocols like OPC, Modbus, Ether TCP/IP, Seri Good to have: Knowledge of Pharma validation process and documentation (GMP/FDA) - Valuable Kepware/Metricon OPC Server knowledge Effective communication and writing skills Don't meet every single requirements? Studies have shown women and people of colour are less More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯

Quality Audit and Compliance (SQ A&C) team, supporting the Global Supply Chain globally. The SQ A&C team ensures quality and compliance throughout the product lifecycle by conducting GMP assessments of quality-critical materials and services across GSK's manufacturing network. The Supplier Quality Audit Lead , reporting to SQ A&C Senior Manager, plays a key role in ensuring … GSK's material and service suppliers meet compliance standards with regulatory requirements and GSK expectations. The role involves planning, executing, and documenting GMP and Quality Systems audits for assigned suppliers, managing supplier action plans to address identified gaps, and maintaining audit data in GSK's supplier management systems. Additionally, the auditor may provide expertise on supplier change controls when needed. … In this role you will Performing GMP/Quality System assessments/audits of assigned suppliers; making risk-based recommendation on supplier GMP approval status (including proposals for continued use of suppliers with marginal compliance) and documenting assessments/audits in relevant systems. Agreeing appropriate corrective and preventive action (CAPA) plans with suppliers and following up on the completion of More ❯

We are seeking a Supplier Quality Audit Lead within the Central Supplier Quality Audit and Compliance team, supporting the global supply chain. The role involves planning, executing, and documenting GMP audits, managing supplier action plans, and supporting change controls. Responsibilities Perform GMP and Quality System assessments of suppliers and recommend approval statuses. Agree on CAPA plans and ensure their timely … risks, escalate high-risk issues, and support inspections. Candidate Profile Basic Qualifications & Skills Experience in regulated environments like pharmaceutical manufacturing. Degree in Life Sciences or related fields. Knowledge of GMP requirements and QMS principles. Proficiency in English. Preferred Qualifications & Skills Experience with API, sterile, parenteral, or biopharmaceutical manufacturing. Auditor certification from relevant organizations. Application Details Deadline: Sunday 31st August. Please More ❯

to working in a customer-focused service business. Accuracy and attention to detail. Excellent customer service and communication skills. Good written and arithmetic skills to comply with audits and GMP standards. Understanding of GMP/GLP standards. Ability and confidence to work alone on a customer site without supervision and as part of a multi-disciplined team. BSc or equivalent More ❯