101 to 125 of 131 GMP Jobs in England

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 »

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 »

abreast of technological and legislative advancements. 4. Engage with stakeholders to translate technical strategies into actionable plans, ensuring compliance with all relevant standards (eg. GMP, SHE, DI.) 5. Drive business growth through digital capabilities, collaborating with cross-functional teams to enhance the company's digital footprint. ROLE REQUIREMENTS: To be …/Data Scripting/Automation/Databasing Key Words: Senior Research Scientist/Digital Technologies/Technical Leadership/Data/SHE Compliance/GMP/Data Integrity/Continuous Improvement/Digital Projects/Cross-Functional Collaboration/Mentoring/Coaching Hyper Recruitment Solutions Ltd (HRS) is an Equal 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 »

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 »

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 »

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 »

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 »

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 »

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 »

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 »

testing intermediates, products and raw materials in line with demand and business requirements. Job Summary: - Follow approved methods and procedures in accordance with cGLP & GMP requirements. - Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements. - Ensure QC documents are complete, accurate and … subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience. - Experience of working in a GMP environment/method development experience/forensic investigation analysis experience. To Apply: For more information, or to apply for this QC Analyst position please contact 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 »

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 »

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 »

Proclinical is seeking a dedicated and innovative Scientist to join an MSAT Cell Process team. This role works closely with the Process Development and GMP Manufacturing departments, contributing to the development of CAR-Treg therapies and the improvement of next-generation products. The successful candidate will have a unique opportunity … therapies. Responsibilities: Provide technical expertise and practical capacity to the MSAT (Cell Process) team. Help with designing, controlling, optimising, and assessing processes in a GMP environment. Lead tasks related to MSAT across a variety of projects, providing technical leadership. Keep detailed documentation up to date and establish relevant SOPs. Collaborate … working with quality management systems (e.g., Q-Pulse). Knowledge of tech transfer and experience working with CDMOs is desirable. Previous experience working with GMP equipment. Ability to perform experiments independently. BSc degree in a relevant study field and relevant industry experience. MSc is beneficial. Interested or know someone who 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 »

week. There will be an on-call rota. Key experience: Previous experience in a hands on engineering position within a regulated industry Experience of GMP is desirable but other regulated standards will be suitable Multi-skilled engineering capability – both mechanical and electrical An appreciation of IT and cloud based systems … a flexible approach to work For further information, please contact Mark Bux-Ryan. Engineering, manager, maintenance, electrical, mechanical, electro, mechatronics, planned, reactive, systems, controls, GMP, regulated, pharmaceutical, manufacturing, ISO, aerospace, food, chemical, quality, standards 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 »