1 to 25 of 76 Permanent GMP Jobs in England

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 »

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 »

corrective actions Collecting micro-samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/fabric audits Temperature checks Quality checks The nature of this role requires a flexible approach to working hours. Core working hours are: Monday to more »

cyclotron manufacturing processes to provide radioisotope for PET radiopharmaceutical production Ensure that the requirements of Cyclotron Preventative Maintenance, Radiation Compliance, Health and Safety, Good Manufacturing Practice and licensing commitments are met Perform manufacture of radioisotopes according to MarketingAuthorisationsand/or Specials license Be on call during the night for manufacturing … Experience in provision of PET radioisotope production for the commercial manufacture of PET radiopharmaceuticals Practical experience of working with ionizing radiation Working knowledge of GMP environment Benefits: 26 days' holiday with the option to buy or sell an additional 5 Up to 10% employer pension contribution Share and bonus scheme more »

area highlighting any stock issues to the engineering team manager To maintain standards of hygiene and good housekeeping appropriate to a quality food manufacturer. GMP standard of workshops and engineers tool boxes is maintained at a high level About you. Strong people management experience A multi skilled background Experience completing 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 »

Note: Applicants must be authorised to work in the UK Our client is a leading pharmaceutical distributor with multiple GDP distribution facilities and a GMP assembly unit. They are committed to maintaining the highest standards of Good Manufacturing and Distribution Practice (GDP) and regulatory compliance. Their dedication to quality, safety … to move forward with your application. Other suitable skills and experience include Responsible Person (RP), Quality Affairs Specialist, Compliance Manager, Pharmaceutical Quality Control Manager, GMP Auditor, Distribution Manager, Pharmaceutical Consultant, Quality Systems Coordinator. more »

are collected for testing schedules and testing schedules are met Logging micro samples Accurate carrying out of positive release checks for all finished products GMP audits/Glass and plastic audits, including generation of improvement areas, completing database Ensure close outs of non-conformances Sampling and recording of finished product more »

you a skilled technical assistant with a passion for food manufacturing? Do you have a keen eye for systems and specifications, and experience in GMP and supplier approval? If so, we have an exciting opportunity for you! About the Role: We are seeking a Technical Assistant for our esteemed client … maintaining high standards and ensuring compliance with industry regulations. Key Responsibilities: Manage and maintain technical systems and specifications. Ensure compliance with Good Manufacturing Practices (GMP). Conduct supplier approval processes and audits. Collaborate with various departments to ensure seamless production and quality control. Provide technical support and expertise where needed. … Requirements: Proven experience in a technical role within food manufacturing. Strong understanding of systems and specifications. Knowledge of GMP and experience in supplier approval processes. Excellent attention to detail and organizational skills. Must have an indefinite right to work in the UK. Why Join Us? Competitive salary up to more »

which will include some weekend working as set by the rota. Day to day duties will be: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and 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 »

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 »

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 »

and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications 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 »

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 »

Desirable) Time served Engineer. NVQ Level 3 Qualification or above Electrical Bias The Role Carry out duties ensuring the site achieves and maintains required GMP standards. Ensure all work conforms to statutory & safety requirements. Ensure that risk assessments are completed and actioned. Carry out site maintenance activities and ensure GMP 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 »

about working together to achieve greatness. As a valued member of our team, you will bring the following skills and experience: - Good Manufacturing Practice (GMP) preferably in chilled food manufacturing Lean Six Sigma Black Belt or level 5 Improvement Specialist Apprenticeship IT Skills including Microsoft Office People Management experience plus more »

work environment and that all tools are maintained and accounted for. Liaise with the SHEQ team to resolve H&S issues, environmental, internal audits, GMP, COSHH and ISO quality issues, and ensure all compliance checks are complete and correctly filled. Attend all nominated training modules as necessary. Undertaking any other 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 »

this time. About The Role Working as a Multi-Skilled Engineer, preferably with an electrical bias you will primarily offer engineering support in the GMP area. You will also handle responsibilities related to site utilities and facilities as needed. Your duties will include completing both scheduled and unscheduled maintenance tasks more »

vacuum cooler. Help with maintaining the plant to ensure we are hitting our consent. Ensure all maintenance equipment is fit for purpose. Compliance to GMP, QMS, 5'S, BRC Person Specification ONC in a related subject or equivalent experience Recognised apprenticeship Experience of working in an FMCG environment Electrical engineering 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 »