11 of 11 GLP Jobs in the UK excluding London

crop transformation platforms or product development pipelines. Hands-on experience supporting vector design for corn, wheat, soybean or other major crop species. Knowledge of GLP, QMS or quality-controlled research environments relevant to commercial product development. Understanding of regulatory, freedom-to-operate, IP and stewardship considerations that influence commercial vector ...

Quality Management Systems at MedPharm. The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems and QA oversight of manufacturing and laboratory activities. … methods, sampling instructions and protocols. Support review of analytical investigations including OOS, OOT and atypical results. Review laboratory documentation to ensure compliance with GMP, GLP and internal procedures. Support QA oversight of reference standards, retained samples and stability documentation where applicable. Materials Management Perform QA review and disposition of starting ...

Oxford. Reporting to the Principal Scientist, you will translate processes into a robust digital platform, collaborate across departments, and help ensure GMP/GLP compliance while driving continuous improvement. A BSc or equivalent is required, with laboratory experience and basic coding knowledge; #J-18808-Ljbffr ...

support accurate, uninterrupted testing. Identify technical issues or result anomalies and take appropriate corrective action. Maintain professional development and complete required training, including ISMS, GLP, CQC, DocuSign and GDPR. Required Skills and Experience: Degree in Biomedical science, biology, chemistry, or a related field. Currently HCPC registered as a Biomedical Scientist ...

digital healthcare and remote patient care. Key Responsibilities Review and assess asynchronous online patient consultations, including weight-management services. Assess patient suitability for GLP-1 therapies and other treatments in accordance with clinical guidelines and prescribing pathways. Request additional clinical information where required to support safe and appropriate clinical decisions. ...

started. Backed by a leading growth equity investor, we’re scaling rapidly and partnering with global leaders such as Prologis, ECE, CTP, Hillwood, Logicor, GLP, and Unibail-Rodamco-Westfield. As we continue to grow through strategic acquisitions and bold innovation, we stay true to our core values: adaptability, collaboration ...

implementation. In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands‐on expertise with a pragmatic, client‐focused consulting approach. What you'll doYou … Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10).Authoring, reviewing and maintaining quality policies, standards, SOPs, forms and controlled ...

Clinical Method Development & Validation Lead We are supporting a GLP-regulated veterinary pharmaceutical company in their search for a Clinical Method Development & Validation Lead to head up their bioanalytical method development and validation team within the GLP Clinical Research section of R&D. This is a hands-on leadership role …/MS), and LC column selection. You'll plan, lead, and manage all bioanalytical method development and validation activity in line with GLP, VICH, and internal SOPs, lead troubleshooting and root cause analysis on new and existing methods, and ensure the quality, accuracy, and integrity of all data and documentation ...

subject matter expert. Optimising analytical extraction techniques, chromatography methods, and LC columns. Managing and mentoring the Method Development & Validation team. Ensuring compliance with GLP, SOPs, and international guidelines. Troubleshooting analytical methods and recommending improvements. Overseeing cost-effective laboratory operations and consumable spend. Writing and approving Methods of Analysis and transferring … analytical teams. Supporting regulatory submissions and resolving regulatory queries. Conducting investigations, implementing CAPAs, and driving continuous improvement. Preparing, reviewing, and ensuring adherence to GLP SOPs. Leading team meetings and staff development sessions. Qualifications Degree in Biochemistry, Biomedical Science, or related field. Required Skills 4+ years in a GxP laboratory (2+ ...

assess the physical properties of medical devices. Scientists will generate, document and analyse data in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). Scientist II’s should also be able to use their knowledge and experience to develop test methods based … present findings of the laboratory. Effective organisation of assigned workload; ensures integrity of all data generated and timely/accurate provision of results to GLP standards. Accurate recording and analysis of laboratory data in accordance with good documentation practices. Perform detailed laboratory investigations to determine the root cause analysis ...

Oxford Nanopore Technologies : Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore-based sensing technology for ...