25 of 25 GMP Jobs in the South East

skills. - Experience dealing directly with customers on quality matters. - Excellent communication and stakeholder management skills. - The ability to work independently while managing multiple priorities. - GMP experience (desirable). - Degree or equivalent in a science, engineering or manufacturing discipline (desirable). This is an excellent opportunity for an experienced Quality Assurance ...

relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485 and 14971, FDA 21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability ...

relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485 and 14971, FDA 21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability ...

relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485 and 14971, FDA 21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability ...

relationship between Complaint Handling, CAPA, Nonconformance and Risk Management processes Knowledge of ISO 13485 and 14971, FDA 21CFR Part 803, 820, 822, 806, EU GMP Annex 11 Proven ability to work both independently and in teams in a dynamic, fast-moving environment Good understanding of SaaS and GxP principles Ability ...

Investigational Medicinal Product (IMP) manufacturing and associated 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 … analytical 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 ...

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. ...

problem-solving skills. Good IT skills, including Microsoft Office and MRP/ERP systems. Desirable 5+ years' mechanical inspection experience. Knowledge of FDA, GMP and ISO 13485 standards. Engineering qualification, apprenticeship, or equivalent industry experience. Experience working within regulated manufacturing environments. Key Skills CMM Programming & Inspection (Essential) LK & Mitutoyo CMMs ...

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 ...

62443Experience with industrial automation systems and OT architecture, including integration with IT systemsFamiliarity with regulated environments and standards such as GxP (including GMP and GAMP5) and IEC 61508/61511Understanding of cyber security risk assessments, controls, and system documentationExperience in system lifecycle management, including validation, change control, and documentation practicesKnowledge ...

responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity Guidance, GAMP5 principles, and applicable global regulatory requirements. The position provides technical oversight of electronic systems, manages validation activities, assesses system … validated state. Identify and close existing CSV gaps to ensure compliance with Annex 11 and data integrity requirements. EudraLex Volume 4 Good Manufacturing Practice (GMP) guidelines, laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/ ...

improvement initiatives, including automation developments and SMED projects. Maintain accurate maintenance records and documentation. Ensure all work is completed in accordance with Health & Safety, GMP, quality and environmental standards. Support colleagues through knowledge sharing and contribute to maintaining high engineering standards across the site. About You To be successful ...

MedPharm Ltd in Guildford is seeking a CSV Specialist to govern and manage validated computerised systems (GxP) across the site, ensuring compliance with EU GMP Annex 11 and MHRA guidance. You will oversee the validation lifecycle (URS, IQ/OQ/PQ, reports), assess updates, perform risk assessments, and support ...

/restore, or diagnostics standards for complex software-enabled products. Experience working in regulated or validated environments, including exposure to SAT, IQ/OQ, GMP, or automation validation practices. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether ...

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 ...

UK. Sitting within our UK Quality function, this role reports directly to the Head of Quality UK and plays a key part in ensuring GMP and regulatory compliance across our network of seven licensed radiopharmacy sites. You will act as a central link between Quality Assurance, Regulatory Affairs, Operations … Quality, Regulatory, or a pharmaceutical discipline. Minimum of 5 years’ regulatory experience, ideally within radiopharmacy, sterile manufacturing or aseptic processing. Proven experience with GMP, MHRA expectations and broader GxP requirements. Experience supporting commercial and IMP product development, including clinical trial supply. Strong understanding of regulatory inspections and authority interactions. Experience ...

Duties will include: Picking and packing customer orders Receiving deliveries and updating inventory systems Stock control, cycle counts and inventory checks Completing production and GMP paperwork accurately Following standard operating procedures Maintaining high standards of housekeeping and safety Working within ambient, chilled and frozen environments when required Supporting the wider ...

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 ...

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 ...

into delivery, processes and capability Own commercial performance, identifying growth opportunities and supporting pitches Provide technical leadership across analytics, tagging, MMM, BI and GMP Lead and develop a senior leadership/practitioner team, with responsibility for a large wider function Represent the data practice with C-suite clients and senior … multiple data/marketing disciplines Agency experience preferred, particularly within the media/marketing ecosystem Technical credibility across analytics, BI, MMM and/or GMP - you don't need to be hands-on day-to-day, but must be able to challenge and guide technical teams A strong commercial track ...

major pitches and working with senior clients to identify opportunities to expand data services. Providing technical leadership across analytics, tagging, measurement, MMM, BI and GMP, with enough technical depth to challenge senior practitioners and make sound decisions. Building and developing the leadership team, creating strong development pathways and succession plans. … discipline. You'll ideally have: Experience leading data or analytics teams across multiple disciplines such as Analytics, BI, Data Science, MMM/Econometrics, or GMP Strong experience managing and developing high-performing teams and senior practitioners. A background in an agency environment would be highly relevant, although strong in-house ...