1 to 13 of 13 GMP Jobs in the UK with Remote Work Options

be responsible for supporting the Quality Management System (QMS) and verifying the adherence of manufactured products for human use, in line with current Good Manufacturing Practice (cGMP). As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous … To be successful in this role, were looking for you to have: A-level qualifications (or equivalent Worked within an established Quality System (e.g. GMP, ISO) Writing and producing scientific reports The following criteria would also be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

related to the instruments You will produce timely and detailed reports for equipment Follow the companys procedures and policies as well as ISO and GMP standards on customer sites You will work closely with the technical team such as Field Application Specialist, Technical Sales Specialist, Technical Support Engineer and Sales … in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc.) Ability to work autonomously and unsupervised more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

Proclinical is seeking a dedicated individual for a Director of Quality Assurance position. This role is integral to our mission of developing solutions for some of the most crucial scientific challenges of our age. The successful candidate will be a more »

company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late stage inclusive of GMP/clinical supply manufacture Experience with regulatory documentation for CMC activities on drug substance, drug product both towards FDA and EMA is mandatory Solid experience … with working in a regulated environment under GxP and with adherence to Company SOPs, policies and guidelines Updated knowledge of ICH GMP is required Excellent communication, presentation, and interpersonal skills. Self-driven and motivated team player Familiar with working in a virtual set-up Fluent in written and spoken English more »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role. Main Responsibilities So, what will you be … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

options. Reporting to: CEO Our client is an innovative biotechnology company based outside of the centre of Cambridge. They specialise in the synthesis of GMP grade gene constructs utilising an enzymatic synthesis. Their technology provides exciting possibilities for ensuring cheaper, faster and more accurate DNA/gene constructs than traditional … transfer activities. As a Director of Manufacturing, you will be responsible for: Continuing the expansion and development of manufacturing processes and frameworks across the GMP cleanroom facilities for DNA production. Supporting technology transfer projects from the research and development teams. This will include the review and submission of SOPs. Spearhead … audits, regulatory submissions etc. Build and oversee cross-departmental relationships with R&D, quality, regulatory teams etc. Lead the daily organisational activities of the GMP team and take responsibility for staff training. Act as a point of contact for external clients with respect to project updates and regulatory plans. Manage more »

Job summary The Vaccine Development and Evaluation Centre department, based at UKHSA Porton, is the UK's largest capability for the handling of dangerous human pathogens and animal modelling of infectious diseases. The capability is used to understand pathogenesis and more »

promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from more »

to detail and flexibility. Strong communication skills. Ability to handle stressful situations and controversial issues. Willingness to learn and develop new skills. Knowledge of GMP, GDPR, LSAS, and ethical trade issues. Key Tasks: Prepare and submit regulatory documentation for market registration. Support root cause identification and solution resolution. Conduct and more »

Private Healthcare + Free Parking + Life Insurance + Pension + Ongoing Training + Progression Are you a Laboratory Manager with a background in GMP looking to join a company that is passionate about revolutionizing cancer therapy? You will take on a leadership role where you will receive full product … Your duties will encompass supervising production operations, resolving issues in cell culture processes, and spearheading quality investigations. Your meticulous oversight will ensure adherence to GMP standards and facilitate the seamless integration of novel procedures. This role would suit a Laboratory Manager with a background in GMP looking to join a … role where you will receive full product training, tremendous growth opportunities all while working hybrid. The Role: Manage T cell-based therapy production, maintaining GMP compliance. Lead production, troubleshoot processes, and conduct quality investigations. The Person: Life Sciences or related field background. Regulatory knowledge of T cell Therapy. Demonstrated leadership more »