9 of 9 Permanent GMP Jobs in the Thames Valley

will be critical as you contribute to process innovations and operational excellence. Here’s What You’ll Need 3+ years of experience in a GMP manufacturing environment This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. ...

conformance, customer complaint investigations, glass & plastic audits, and fabrication audits. - Supporting the training of staff and verification against CCPs, policies and procedures. - Conducting internal GMP audits across departments and conducting hygiene verifications. - Assisting with external audits. The role will be a mix of factory and office-based work to meet ...

beneficial.Experience working with health authorities and supporting regulatory discussions and responses, underpinned by a solid understanding of global development and post-approval requirements, GMP expectations and regulatory practices in at least one ICH region.Able to analyse technical data, create clear regulatory narratives, identify gaps early and manage traceable content across ...

multi-tenant campus to ensure uptime and regulatory compliance. The role requires experience with BAS, CMMS, and building automation, plus strong knowledge of GMP requirements and safety protocols. A relevant engineering degree and industry certifications are preferred. #J-18808-Ljbffr ...

Responsibilities: Under general direction, provides support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs) Participates in project teams to provide review and approval of project Validationdocumentation according to applicable approval matrix ...

Vifor is seeking a Quality Systems professional to support GMP-compliant quality systems across validation, calibration and document management. You will contribute to internal audits and continuous improvement programs while ensuring alignment with FDA/EMA requirements. The role involves collaboration with project teams and serving as a subject matter ...

solution preparation. Ensure top-tier standards by performing visual and instrumental checks on raw materials and finished goods in line with Good Manufacturing Practice (GMP). Maintain a clean, pristine workspace following 6S principles and COSHH/EHS safety guidelines. Use digital interface systems (HMI, POMS, ETMS) to log batch ...

visual and instrumental inspections of raw materials and finished goods. You'll play a vital role in identifying defects and maintaining Good Manufacturing Practice (GMP). Safety & Standards: Maintain a "Safety First" mindset by adhering to COSHH and EHS guidelines and keeping your workspace pristine using 6S principles. Data Integrity ...

Lonza in Slough is seeking a Scientist for QC Product Testing & Stability to perform analytical testing of therapeutic protein samples in a GMP environment. You will apply HPLC, capillary electrophoresis, spectrophotometry and other methods, review data against specifications and contribute to stability studies and quality investigations. The role is site ...