1 to 25 of 81 GMP Jobs in England

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 »

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 »

Proactively address stakeholder concerns, resolve conflicts, and facilitate effective communication channels throughout the project lifecycle. Quality Assurance and Compliance Ensure compliance with regulatory requirements, GMP, and other relevant standards within the pharmaceutical industry. Implement robust quality assurance processes to monitor and evaluate project deliverables, ensuring adherence to specified quality standards. 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 »

inspections to the production and technical teams. Routine checks of production paperwork to ensure all paperwork is completed accurately. Completion of Internal audits including GMP audits, glass and brittle plastic, hygiene etc. including liaising with line managers and production teams to review non-conformances raised and ensuring actions are closed more »

changes). This will require close collaboration with Product Development, Production and QA groups on NPIs using product lifecycle approach, preparation and approval of GMP documentations to support such projects, scheduling, raw material acquisition, supervising engineering batch manufacture, etc. Identifying potential process improvements for existing commercial products including proposals for more »

changes). This will require close collaboration with Product Development, Production and QA groups on NPIs using product lifecycle approach, preparation and approval of GMP documentations to support such projects, scheduling, raw material acquisition, supervising engineering batch manufacture, etc. Identifying potential process improvements for existing commercial products including proposals for more »

monitoring good manufacturing practices, applying HACCP principles and preventing reoccurrence of non-conformance against these standards. To audit compliance against Quality Management Systems and GMP, raising all non-conformances against relevant standards with objective evidence enabling the operational teams to take the appropriate and necessary corrective action, to follow up more »

of Validation Proven leadership skills. Computer literate with the ability to use CRM systems Experience and knowledge of H&S, COSHH, ISO, GLP and GMP A problem solver Due to the nature of the role, you will need excellent colour vision If you believe you meet the above criteria and 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 »

be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT skills Important Information: We endeavour to process more »

Safety Compliance Ability to manage time and workload effectively. Ability to communicate effectively with stakeholders on all levels. Proven industry experience from a regulated GMP manufacturing environment Interrogation of multiple OEM software packages. Ability to amend and improve process controls. Experience of driving continuous improvement projects Desirable but not essential more »

miles from Peterborough and 12 miles from Spalding. About the role. 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 site more »

standards and key performance indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab 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 »

and building effective working relationships internally and externally to the business. Desirables: Experience installing equipment in a comparable process industry. Experience working in a GMP environment. AutoCAD user to produce PFD/P&IDs Knowledge of DSEAR, ATEX, Pressure systems, PUWER or other regulation. Root Cause Analysis or other problem 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 »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and 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 »

Pharmacy or Pharmacy Technical Services, particularly chemotherapy; or clinical pharmacy experience across a range of specialised areas (Band 7) Knowledge of Good Manufacturing Practice (GMP) and professional standards (Band 7) Desirable Working knowledge of systemic anti-cancer treatments and supportive care Post-registration experience in Cancer Pharmacy, or Pharmacy Technical … Services particularly SACT; or clinical pharmacy experience across a range of specialised areas (Band 6) Knowledge of Good Manufacturing Practice (GMP) and professional standards (Band 6) Skills and abilities Essential Good oral and written communication skills, including the ability to communicate complex information Methodical and accurate Ability to assess priorities more »

site & escalate/action where necessary Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP/Glass and Hard Plastic and Fabrication audits Carrying out sampling and swabbing & leading on investigations corrections -preventative procedures To be the subject matter expert more »

site & escalate/action where necessary Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP/Glass and Hard Plastic and Fabrication audits Carrying out sampling and swabbing & leading on investigations corrections -preventative procedures To be the subject matter expert more »

least 3 years industrial experience and be able to work on a number of product development projects. Previous industrial experience within a regulated environment GMP environment, pharmaceuticals, food, electronics . Demonstrate project control, with evidence on how you achieved the business goal. Provide support to design operatives to aid in more »