101 to 125 of 130 GMP Jobs in the UK excluding London

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 »

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 »

compensated at an enhanced overtime rate) Experience in some or all of the following areas is highly desirable: ISO 9001 Quality systems Working under GMP conditions Maintaining and certifying equipment to British, European, or International Standards (BS EN 12469, ISO 14644, HTM03-01, GMP) PLC-based control systems IIE 18th more »

by performing physical and analytical testing and report accurate results. Duties to include: Being responsible for physical analytical testing. Follow internal methodologies. Adherence to GMP requirements. Accurately record microbiological results within data packages, as received. Execution of protocols. Ensure laboratory housekeeping standards are maintained and documented accurately. Ensure all equipment … detail, able to prioritise workload, positive and flexible approach. One to two years' experience in a similar role would be ideal, but not necessary. GMP experience would be desirable. CVs in Word please. New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. Committed to diversity, equality and opportunity for more »

Lab Analyst/Senior Lab Analyst Serving Society through Science, Tata Chemicals Europe (TCE) is one of Europes leading producers of sodium carbonate, salt and sodium bicarbonate and other products, from our plants in Cheshire, UK. British Salt has been more »

of Quality Assurance/Quality Control during times of absence. Responsible for the direct line management of technicians and assistants. Provide initial and refresher GMP training to all aseptic staff, to ensure a thorough understanding of the importance of GMP. Person Specification Qualifications Essential NVQ Level 3 in Pharmacy Services … and Dispensing of Medicines" (or willingness to undertake in first year of role) Current registration with the General Pharmaceutical Council Knowledge and understanding of GMP, GLP and Pharmaceutical Quality Systems Knowledge Essential Demonstrable post qualification experience particularly in the specialised area of Aseptic Services and Pharmacy Quality Assurance Experience of 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 »

site in Loughborough, you will be responsible for conducting chemical testing following set procedures, maintaining accurate records of work and conducting all analysis following GMP and/or internal procedures. This will include undertaking the chemical analysis of raw materials, intermediates and products according to set procedures and methods, as … environment. Experience in analytical techniques (UV, IR, KF, HPLC, GC and dissolution analysis). Previous experience with analytical method transfer and validation. Experience in GMP raw material testing for API, Excipients & packaging Experience in the use of LC-MS systems Experience of conducting cleaning validations and verifications Reward For the more »

in industry? Or do you already have a background in an industrial chemistry lab but would like to develop your skills further in a GMP environment? SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst – Level 1 Synergy … instruments, software packages and other analytical techniques (E.g. Empower 3). Is proficient in problem solving and may have expertise in troubleshooting analytical equipment. GMP experience would be desirable. more »

the requirements and standards for the operation of Aseptic Services? Awareness of current developments in aseptic services/Good understanding of Good Manufacturing Practice (GMP as described in the Orange Guide/Aseptic Services. Laws relating to Pharmacy Practice) Advanced knowledge of a specific clinical area/Excellent communication (verbal more »

to manage/adjust timelines and priorities; escalate issues and concerns as they arise. Ensure all activities are delivered compliant to defined processes and GMP; concerns/risks are identified. Ensure appropriate and complete records arising through operational activities are maintained and TPCs in compliance with GMP and that meet … commitments meet agreed timelines and quality KPIs. Interim Packaging Project Coordinator - The Skills You'll Need to Succeed: Experience working in an R&D GMP environment. Experience working in an operational Packaging Labelling Distribution (PLD) role within Clinical Trial Supplies. Knowledge of Clinical Trial Supply CMOs and their capabilities Knowledge … of the pharmaceutical and clinical development processes and their relationship to the clinical supplies delivery processes; aware of clinical supply GMP requirements and standards. Lean Sigma training/experience Project Management training/experience Experience demonstrating organizational and planning skills coupled with strong written and oral communication skills Demonstrated capability more »

factory. Monitoring customers returns and give daily the report to finance team. To ensure that all operatives and staff within the factory comply with GMP and hygiene procedures and to advise and give training when this is not the case. To work effectively within the departmental rota, ensuring all aspects … company procedures and policies. To monitoring, verify and report any issues daily on Day & Night Shifts check list Compliance Audit. To carry out Internal GMP/Glass and Hard Plastic Audit within the factory. Weekly monitoring of all PPE request orders. To ensure that all operatives and staff within the … factory comply with GMP and hygiene procedures and to advise when this is not the case. To actively partake in the resolution of quality related issues. To support training all members of staff in food hygiene, health & safety, manual handling, fire safety, chemical safety, and allergen awareness training. To assist more »

growing portfolio of its own products? Working on a SME facility, you will have the perfect opportunity to gain fantastic exposure in an industry GMP setting that will provide development and advancement opportunities. Whilst the duties may seem routine – testing pharmaceutical and personal care products using GC, HPLC and various … two hires will be made in this round of recruitment. Key experience: Previous QC or analytical chemistry experience essential Must have worked within a GMP or GLP setting An understanding of raw materials and finished product testing Experience in some of the following will be important – HPLC, GC, UV, FTIR … Ryan. Quality, control, qc, analytical, chemistry, HPLC, chromatography, GC, gas, high, performance, liquid, testing, product, raw, materials, pharmacopoeia, FTIR, UV, bench, laboratory, analyst, technician, GMP, GLP, manufacturing, pharmaceutical more »

instruments to identify profiles of 'unknown' organic compounds and mixtures, ensuring safe and compliant disposal. Follow approved methods and procedures in accordance with cGLP & GMP requirements. Ensure all Health, Safety, and Environmental standards are met, including workplace organization, work instructions, risk assessments, COSHH assessments, and housekeeping. Participate in method development … Analyst . Skills and Qualifications: Education: Degree in Chemistry. Experience: Minimum 2 years as a QC Analyst in the Fine Chemical or Pharmaceutical industry (GMP/GLP environment). Technical Skills: Proficiency in forensic investigation techniques such as HPLC, GC, GC-HS, LC-MS, GC-MS, FT-IR, XRF, RAMAN more »

being made correctly Write reports on the analysis carried out for CofAs. Ensure that the testing done is carried out to the required standard (GMP, GLP, MHRA etc). What do you need to be considered? You will need: Degree or equivalent experience in science-based subject, ideally Chemistry. Working … Experience of analysing organic compounds such as fine chemicals, petrochemicals, or APIs. Knowledge of working in a regulated laboratory and standards such as UKAS, GMP, GLP, MHRA, FDA etc. What to do next? Interested? Of course you are, who wouldnt want to work for a great company with a supportive more »

focus on compliance within a specific bakery, working with the teams to identify non-compliance and full engagement and support to ensure company processes. GMP and procedures are fully understood. Work with the bakeries to ensure compliance with relevant customer standards and codes of practice. Conduct physical factory audits (outside … safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and any non-conformances raised to bakery management. Verify that close out actions are robust and complete. Communicate 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 »

proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products andstability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process … timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and … and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Essential Experience Experience within a QC laboratory working to GMP within a recognised quality system. Ability to organise work within a busy laboratory with experience of writing and working to SOP documentation. Knowledge of GMP more »

washing bottles, using the autoclave, re-stocking labs, weekly and monthly cleaning maintenance. Moving onto regulatory testing when competent and trained. Good Quality Manufacturing (GMP) training will be given as we are inspected by the MHRA. Will be expected to adhere to ALCOA+ GMP rules of accuracy and record keeping. more »

and collaboration with Operations and Quality teams. Major Responsibilities Under the QC Manager's direction, the Incoming QC Team Leader will: Ensure GDP/GMP compliance within Incoming Inspection and Quarantine areas through inspection of incoming goods against specifications. Create and maintain incoming inspection procedures and work instructions. Manage QC … external audits (e.g., BSI, FDA). Support and complete other tasks set by the QC Manager. Skills and Experience Working knowledge of GDP/GMP requirements. Ability to create and write Standard Operating Procedures and Work Instructions/Specifications. Understanding of inspection criteria and the use of drawings/specifications. … area for medical devices. Knowledge of SAP (desirable). Knowledge of Master Control (desirable). Strong written and oral communication skills. Good understanding of GMP compliance requirements in Quality Control. Attention to detail. Promotes a collaborative working environment. Understanding of using basic measurement tools (e.g., calipers/jigs and gauges more »

cell therapies for established applications as well as first in man studies. Main duties of the job In this role you will be performing GMP production and interpreting novel recombinant proteins or Cell and Gene therapy clinical grade products manufactured on behalf of NHSBT for clinical trials. Operating a range … Post holders will work at the level of responsibility and to the standards of conduct and performance expected of a graduate Scientist. Following initial GMP production ensure any subsequent follow up investigations or actions are identified and initiated. Communicating complex information, including technical and scientific analysis, verbally, in writing and … electronically. Contributing to the GMP production service leading to release of reports or products. Assisting in training and supervision of support staff. You will be required to travel and spend time away from base, which will involve working irregular hours and overnight stays when required, with prior notice. You will more »

and released in compliance with the relevant regulatory standards and our high-quality benchmarks. Key Responsibilities: Certify batches for release, ensuring compliance with EU GMP and relevant regulatory requirements. Conduct audits, both internally and externally, to ensure adherence to quality standards. Collaborate with various departments (eg, Manufacturing, Quality Control, Regulatory … Affairs) to ensure quality assurance throughout the product life cycle. Provide expert guidance on GMP and regulatory compliance issues. Lead and support continuous improvement initiatives in quality systems and processes. Handle deviations, investigations, and CAPAs effectively, ensuring root cause analysis and implementation of corrective actions. Requirements: A valid QP status more »

role for you! As a Technical & Quality Coordinator, you will be: Updating and developing technical documentation. Ensuring the organisation remains compliant with food safety, GMP, quality, ACCP , and health and safety procedures . Conducting, and supporting with, internal and external audits and finished product traces . Recording all findings and … in food science or related field. Previous experience in a Quality & Technical role within food manufacturing . A strong understanding of HACCP, BRCGS, and GMP standards and food legislation . Computer literate with MS Office. Able to work well independently and part of a team. If you believe you meet more »

its capabilities. This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying … protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline Qualifications related to validation and quality compliance (GMP/ICH/FDA/USP/EP policies). Experience of validating manufacturing/laboratory equipment, facilities/utilities and processes, including the generation more »

Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »