51 to 75 of 98 GMP Jobs in the UK

ready state. Who you are: - Ideally degree qualified in life science or equivalent qualification, you will have worked in a similar position within a GMP or other highly regulated environment. - You will possess effective numeracy and literacy skills and be well versed in ensuring accurate work is always maintained. - Previous more »

safety compliance. Lead and investigate safety incidents to ensure compliance with standards and close out actions. Oversee and manage process control automation in a GMP-regulated manufacturing environment. Lead WAH activities and projects to improve WAH tasks, and support high-pressure washing activities. Ensure compliance with packaging, transport of dangerous more »

established technical Laboratory background including proven experience of GC (Gas Chromatography) and HPLC. Experience dealing with analytical reports and instrumental trouble shooting on a GMP site as a QC Analyst is also essential. For this QC Analyst role please apply directly. more »

PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous more »

as developing action plans to drive improvement. Your main accountabilities will include: Participate and direct QA team to observe and audit production processes and GMP, ensuring products are made to specification and within customer codes of practice and Bakkavor standards, reporting findings to managers as appropriate Assist in delivery of more »

and on into production phase 1 to 3 to ensure competent technology transfer of drug products Experience in completing manufacturing documentation in accordance with GMP Desirable Criteria (The following criteria may be applied if a large pool of applicants exist) Previous experience within a technical role in the pharmaceutical industry 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 »

safety assurance and business improvement processes for the site. This role is instrumental in driving our food safety agenda, leading quality standards and site GMP to drive down complaints and costs, as well as ensuring full compliance with relevant Legal, National, Corporate, and Retailer standards. To excel in this role more »

operating procedures currently in use, and verifying that study documentation meets the requirements for compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards. You will manage your workload to ensure that tasks are adequately resourced and scheduled efficiently and effectively, with all work audited and carried out … in line with GLP and GMP principles. You will provide compliance advice and guidance to staff when needed and support Study Directors in resolving issues and discussing projects with clients. Additionally, you will engage with clients regarding any deviations, investigations, or out-of-specification events to ensure that any resulting more »

laboratory tasks and data analysis promptly and to an exceptional standard, adhering to all relevant procedures, Study Plans, and SOPs. - Comply with GLP/GMP standards, ensuring all activities meet health and safety guidelines and understanding all risk assessments related to the tasks (COSHH, GMO, etc.). - Maintain GMP compliance more »

pharmaceutical, biotechnology, manufacturing). Knowledge of regulatory requirements and compliance standards relevant to laboratory operations (e.g., FDA 21 CFR Part 11, ISO 17025, GLP, GMP). Experience with relational databases Oracle, SQL Server, Postgres. Experience with cloud services and infrastructure highly desirable Excellent problem-solving skills and ability to analyze more »

team. Ensure all Radio pharmacy work complies with statutory regulations and good practice codes; the latter including. The EU Guidance on Good Manufacturing Practice (GMP)/Rules and Guidance for Pharmaceutical Manufacturers and Distributors published by the MHRA. Define, in conjunction with the Head of Nuclear Medicine, Radio pharmacy production … relevant business cases, financial planning and clinical governance where new service developments are proposed. Together with the Head of Nuclear Medicine and the trusts GMP Quality controller act as the Trust expert for the safe use and introduction of all radiopharmaceuticals. Manage specialist staff rotas/leave arrangement to ensure … good scientific knowledge (degree level). An in depth knowledge of the theory and practice of radiopharmaceutical production Detailed knowledge of Good Manufacturing Practice (GMP) An in depth knowledge of the practices and procedures associated with the use of radiopharmaceuticals for routine nuclear medicine investigations A good knowledge of the more »

pharmacists to ensure efficient transfer of drug related care Be aware of, and apply, relevant legislation such as the H & SAWA, COSHH, Medicines Act, GMP etc. At all times practice in accordance with the Code of Ethics of the General Pharmaceutical Council Person Specification Experience Essential Womens and Children's 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 »

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 »

Able to demonstrate knowledge of clinical trial processes, including relevant legislation and local policies (Band 6) Able to demonstrate specialist clinical trials knowledge (GCP,GMP), relevant or applicable to the job role, underpinned by theory or relevant practical experience (Band 5 & 6) Developed IT skills Desirable (Band 5) Able to … demonstrate knowledge of clinical trial processes, including relevant legislation and local policies (Band 5) Able to demonstrate specialist clinical trials knowledge (GCP,GMP), relevant or applicable to the job role, underpinned by theory or relevant practical experience (Band 5) Appropriate Short Management Courses e.g. Appraisal training, Leadership skills (Band more »

company dedicated to improving health and wellness through cutting-edge products. Committed to excellence, they operate to the highest standards of Good Manufacturing Practices (GMP). Key Responsibilities: Oversee and maintain the Quality Management System (QMS) to ensure compliance with GMP standards. Conduct thorough internal audits and participate in external … reviews to identify areas for improvement and ensure continuous quality enhancement. Collaborate with cross-functional teams to implement quality processes and provide training on GMP compliance. Develop and update quality policies, procedures, and documentation to align with industry best practices. Requirements: Bachelor's degree in a relevant field (e.g., Life … Sciences, Pharmacy, Quality Management). Proven experience in quality systems management within the Medical Nutrition or Pharmaceutical industries. In-depth knowledge of GMP standards and regulatory requirements. Strong analytical skills with a keen eye for detail. Excellent communication and interpersonal abilities to work effectively with various teams. Experience in leading more »

QA role in Pharma R&D, Infrastructure and Validation team, you will perform the quality assurance activities and quality oversight of the Validation and GMP facilities management activities performed within Pharma R&D across the UK sites. In this role you will be key in the following areas… • Providing review more »

safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift ... more »

co-ordinate the day to day workload, ensuring items are manufactured in a timely manner and colleagues are supported. To follow good manufacturing practice (GMP) at all times. To generate worksheets and labels, ensuring medicines are charged correctly using the pharmacy computer system. To in process check worksheets and labels more »

of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply 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 »

under of 'specials' licence. You will have a key role in ensuring all units with Pharmacy Technical Services are compliant to Good Manufacturing Practice (GMP). About us University Hospitals Bristol and Weston NHS Foundation Trust (UHBW) is one of the largest acute Trusts in the country, bringing together a … responsibilities, please refer to the job description document attached to this vacancy. Person Specification Knowledge and Experience Essential Basic knowledge of Good Manufacturing Practice (GMP) Basic knowledge of Good QC Laboratory Practice (GQCLP) Experience of working in a laboratory undertaking analysis Desirable Experience of aseptic preparation Knowledge of COSHH & health more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and more »