1 to 25 of 42 Permanent GMP Jobs with Hybrid or WFH Options

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

and annuity systems by designing, specifying and querying SQL data and reports, supported by the use of a bespoke Data Analysis and Reporting Tool GMP rectification and GMP equalisation Prepare data for client reporting Produce calculation specifications based on Trust Deed and Rules for various pension schemes Create calculation proforma more »

build brighter futures for colleagues, clients and communities. The role will form part of the projects team with the current focus being around delivering GMP Equalisation projects on the proposition to clients, which can incorporate or lead onto being involved in de-risking projects for clients over time. This is … with internal teams to deliver a streamlined service to other lines of business. Directly involved with the management of more junior colleagues within the GMP Equalisation team, including supporting with performance reviews, training, and personal development plans. Develop skills to support on various consulting aspects of GMP projects and have … in Pensions, with a focus on Technical aspects and solid exposure to consultants and broader client support teams. Experience of technical calculations required for GMP Rectification and Equalisation projects. 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 »

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master 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 »

linked to an office and will require occasional visits from time to time. Remote opportunities currently include: Administration Projects Team - All levels - Work includes: GMP rectification/equalisation, Buy-in/Buy-out, Data Cleansing, Ad hoc projects for example scheme closures, benefit rectifications, liability reduction exercises, McCloud, Pension Dashboards. more »

the review of manufacturing and quality control records. Contribute to the preparation, review, and upkeep of product specification files. Provide quality support on various GMP studies. Manage the audit program including execution of internal and external audits. Monitor and support risk management activities. Maintain knowledge of existing and emerging industry … programs. Offer specialist advice to all team members to enable operational efficiency. Requirements Strong experience in GCP QA, helping implement QMS. Good understanding of GMP/GLP. Experience managing vendors and clinical trial. Apply now If you are interested in learning more or applying to this exciting opportunity then please more »

as a subject matter expert (SME) on all contamination control activity and processes. Develop, monitor, improve and maintain procedures to ensure compliance with Good Manufacturing Practice (EU/FDA and other appropriate standards) for the manufacture and testing of pharmaceuticals. Ensure all testing is carried out as per the approved … testing methods (including validation and transfers). Ensure batch certification duties in accordance with relevant procedures and provide support to the Qualified Person for GMP Compliance and Certification. Collaborate with an organization’s technical and supply chain departments manager to ensure materials from external suppliers meet quality requirements as defined 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 »

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 »

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 »

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 »

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 »

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 »

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 »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »

with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project … with facilities design, engineering, and/or construction methods and procedures, including experience working with various project delivery methods (low-bid, Gross Maximum Price GMP/construction at risk, or Integrated Project Delivery IPD ). Architectural design, corporate real estate, facilities engineering, and/or construction management supervisory/project more »