22 Permanent GMP Jobs in London

always opportunities to learn and gain exposure. Experience: Previous experience in a QA position within a pharmaceutical, healthcare or food setting Working experience of GMP Operational Quality Assurance experience including batch review/release Exposure to handling complaints processes Lifecycle experience of deviations, CAPAs and change controls Strong stakeholder management … Mark Bux-Ryan for further information quality, assurance, QA, QC, control, analytical, chromatography, HPLC, laboratory, documentation, analyst, officer, specialist, executive, administrator, good, manufacturing, practice, GMP, GLP, audit, SOP, training, complaints, batch, review, release, CAPA, deviation, change, control more »

Lead best practice in the department and become a key contact for the mentoring and training of more junior members of staff. Act as GMP ambassador, take responsibility for ensuring GMP compliance and adoption of GMP principles e.g., right first time. Lead activities to ensure close working with Analytical development … understanding of cell biology and immunology (preferred) Strong verbal and written communication skills. Flexible, self-motivated, and focused on team outcomes. Strong understanding of GMP regulations. Excellent organisational skills with the ability to present results clearly and logically, working co-operatively as part of a team, as well as independently. more »

opportunity to contribute to the advancement of cutting-edge T cell therapies for the treatment of serious medical conditions. Responsibilities: Batch Manufacturing within a GMP setting Support the scale up of Manufacturing operations in line with GMP standards Draft and maintain SOP’s and batch records Recording all activities and … Support and mentor more junior members of staff Qualifications: BSc or MSc degree in a Biological Science, Biotechnology, Immunology related field Experience in a GMP Manufacturing environment Background in laboratory operations – Immunological cell-based assays Good understanding of and skilled with multi-parameter Flow Cytometry Work co-operatively as part more »

analytical team to contribute to the overall group objectives and development of staff. Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements … Proven track record of managing a team within a cGMP QC analytical environment. Degree in a relevant scientific discipline or equivalent experience. Understanding of GMP requirements e.g. legislation, guidelines and requirements related to Gene Therapy, QC method qualification and validation, QC processes, equipment and systems, including Computer System e.g. of … EU GMP requirements for Advanced Therapy Medicinal Products, EU/FDA GMP guidelines, EU Annex 1, EU Annex 11 & CFR Part 11 and ICH guidelines Q1-Q10. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy more »

role will be joining the UK team, as a senior individual contributor and part of a global team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMS system Able to manage non-compliance issues and … requirement will be that you are able to travel to West London site and to supplier sites. It is a must that you have GMP and GDP experience. The role will be joining a team which is integral to the business and requires strong communication skills. The team are close more »

qualifications and experience: 5 years experience in an environment associated with the manufacture, testing, and dispensing of radiotracers. Relevant experience of Good Manufacturing Practice (GMP), typically 2 years post qualification. Experience of working in Radiotracer production facility, Aseptic service or similar environment. Experience supervising technical staff and management of resources. 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 »

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 »

will conduct, coordinate and support quality aspects of the Company business operation, ensuring quality compliance throughout the business with focus on WDA, MIA and GMP and GDP activities. Key Responsibilities: To ensure that a quality management system is implemented and maintained and appropriate to the activities at the Company inclusive … EU Guidelines on Good Distribution Practice of Medicinal Products for Human Use (2013/C343/01) and EudraLex – Volume 4 – Good Manufacturing Practice (GMP) guidelines. Providing compliance support and spreading the quality culture throughout the company. Maintain processes (GMP documentation lifecycle, Change Control, Deviation, CAPA, self-inspections, Complaints, GMP … the role of the enforcement group, the Inspection Action (IAG) and resulting actions that can be taken due to non-compliance. Good understanding of GMP/GDP. Excellent attention to detail. Effective time management. Self-motivated & highly target driven. more »

Job summary This position presents an exciting opportunity for an experienced radiochemist or radiopharmacist proficient in PET radiopharmaceutical production to GMP standards. As the Production Manager, you will lead our team of radiochemists at the Positron Emitting Radiopharmaceutical Laboratory (PERL), located within St Thomas Hospital. The ideal candidate must possess … expert knowledge in relevant regulatory governance areas, particularly Good Manufacturing Practice (GMP), as well as Health and Safety, Environmental Safety, and Radiation Protection Regulations (IRR2017 and IR(ME)R). This expertise will ensure adherence to these regulations within the PERL facility. Main duties of the job The role entails … managing radiochemists within PERL to ensure timely, safe, and efficient completion of production duties. Emphasis will be placed on compliance with GMP regulations, development of new procedures and radio tracers, and streamlining processes while maintaining safety standards. This includes supporting the installation and validation of new production equipment. The successful more »

track record in this regard. Exhibit adept conflict resolution skills, further enhancing your capacity to lead effectively. Have experience working within environments governed by GMP regulations (at least 4 years). How to Apply: Don't miss out on this amazing opportunity! Submit your application. more »

global footprint. The Head of QP will be a key position within the Quality and Manufacturing organisation, acting as a subject matter expert for GMP and managing a team of QP professionals to prioritise varied complex projects. This position will be reporting to the VP of Quality and is seen … the core function of batch disposition to guarantee the quality and safety of the products You will be the key subject matter expert for GMP, providing guidance and expertise to support the manufacturing operations Assisting in regulatory and compliance activities, ensuring adherence to industry regulations and standards whilst being able … potentially global scale Maintaining a strong presence on the shop floor whilst actively engaging with operational teams to enforce a culture of Quality and GMP excellence. You will develop, mentor and train across the Quality and Manufacturing operations whilst leading by example to foster a GMP and Personal Development culture more »

product.The role will be joining the UK team, as a senior individual contributor and part of a global team.Other essential responsibilities include:Management of GMP and GDP complianceManagement of complaints, CAPAs, risk assessments, and validation protocolsReview and manage the QMS systemAble to manage non-compliance issues and escalate when neededHave … the requirement will be that you are able to travel to West London site and to supplier sites.It is a must that you have GMP and GDP experience.The role will be joining a team which is integral to the business and requires strong communication skills. The team are close-knit more »

Job Description TechYard Recruitment is currently working with a global consultancy who are building a new GMP practice. They are hiring for a Programmatic Consultant. This person will be a programmatic subject matter expert. This is a client-facing role that will be responsible for several strategic initiatives across the … programmatic and GMP/GCP landscapes. These include collaboration on product strategy/vision, client-direct consultancy, license reselling, and internal and external training/education. This is a consultative role and the candidate will not be directly responsible for any media trading or activation. The ideal candidate will have … of channels, very strong analytical, and writing skills, and the ability to make clear, concise presentations. They will have extensive hands-on experience using GMP products and will be individually certified in the use of DV360 and other relevant GMP technologies. Most importantly, they must possess a strong inner drive 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 »

in GCP Quality Assurance within the Pharmaceutical Industry. Strong knowledge of Quality Management Systems within the Pharmaceutical industry. Strong knowledge of ICH-GCP and GMP guidelines. Experience hosting, supporting and preparing MHRA inspections and auditing IT systems. Experience organising and performing internal and/or vendor audits. Experience working in more »

Responsibilities: - Perform environmental monitoring of the aseptic manufacturing facility and ensure all testing aligns with the Environmental Monitoring programme. - Maintain QC facilities to meet GMP requirements and conduct necessary checks to support health authority visits. - Operate and maintain laboratory equipment, ensuring all equipment is calibrated and suitable for use. Requirements … Microbiology or equivalent relevant work experience in a regulated industry (i.e. pharmaceuticals, biologics, or medical devices). - Proficiency in Microsoft Office and knowledge of GMP/GLP regulations, FDA regulations, etc. - Strong problem-solving skills, analytical abilities, and a keen eye for aseptic behaviour. If you are interested in learning more »

products reach every corner of the globe with precision and efficiency. Be the guardian of quality, ensuring every launch meets the gold standard of GMP and GDP regulations. Tackle challenges head-on, turning obstacles into opportunities for innovation and growth. Keep stakeholders in the loop with your expert communication skills … Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products would be advantageous. Great communication skills, coupled with the ability to navigate complex challenges with more »

of Quality Assurance principles within the Pharmaceutical Industry. Strong understanding of Quality Management Systems in the pharmaceutical sector. Thorough familiarity with ICH-GCP and GMP guidelines. Experience in hosting Sponsor audits and/or Regulatory inspections. Demonstrated ability to organize and conduct internal and/or vendor audits. more »

other DSP, Facebook, Twitter Experience of managing vendor relationships Regularly contributes to platform best practices and campaign processes Experience with Google stack and have GMP & Adwords certifications (desirable) Experience with running campaigns across multiple countries/languages Experience with managing a mid- to large-sized team across a range of more »

Job summary This post is a Quality Assurance post specialising in Quality Management/GMP Documentation control and Quality Control. The post holder be part of the QA team, they will manage the Quality Management and Documentation control systems across the directorate and potentially across Kings Health Partners (KHP) The … in line with current guidelines. To support the day to day operation of Q-Pulse. To manage the review and approval process for all GMP documents. Reviewing WFI and microbiological environmental monitoring activities as required. Reviewing EM data and preparing quarterly and annual environmental monitoring reports. About us Guy's … Pulse electronic Quality Management System. To support the day to day operation of Q-Pulse. (Using Q-Pulse) to maintain version control of all GMP documents. To manage the review and approval process for all GMP documents. To progress the development and review of new and updated documents. To provide more »

record in Leading the HSE function across multiple companies in a Pharmaceutical environment. It is key that you have experience within a GXP/GMP environment. Purpose of the Job Health, Safety & Environment Lead and provide oversight and Global strategic leadership covering health, safety, and environment across the Pharmaceutical account. more »