21 of 21 Remote GMP Jobs in the UK

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 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 ❯

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 ❯

in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National Regulatory Authority (AIFA) and is compliant with the FDA 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 ❯

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 ❯

of key information governance services, specifically DHCW's Data Protection Officer service for Clusters, along with providing support to the wider Data Protection Officer service for General Medical Practices (GMP's) and Community Pharmacies. The ideal candidate must be dynamic and have a flexible approach to working, along with excellent communication and organisational skills, in order to provide a first 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 ❯

toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology Basic knowledge of FDA and international medical device regulations/directives and working knowledge of GMP/ISO/GLP guidelines as applied to medical device testing and documentation. Have the ability to work with people and teams in a complex, changing environment and be able More ❯

an award-winning and growing business In addition, you'll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement The 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 ❯

plans that can be presented clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher landscape Are analytical, flexible and 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 ❯