23 of 23 Permanent GMP Jobs in the South East

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. ...

operations Excellent knowledge and understanding of Lab systems, Lab data, and the workings of a lab on a day-to-day basis in a GMP environment (Pharma or Consumer Health Care business). Understanding and experience in the deployment of key lab digital systems (e.g. QC E-planning, QC Electronic ...

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 ...

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/ ...

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 ...

backup/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 ...

/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 ...

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 ...

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 ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

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 ...

audit events, conversions, and consent, server-side GTM evaluation, manage parameter standards and de-duplication rulesPlatform integrations: Build robust connectors/APIs for GA4, GMP (CM360/DV360/SA360), Meta and other platforms. Unify with Databricks, COGNOS and SalesforceData engineering: Model clean tables/views, implement data quality checks … Science, Analytics or Data ScienceProfessional Experience: 6-8 years in analytics/data engineering or marketing analytics engineering rolesExpertise in GTM/GA4/GMP/Meta tracking; strong SQL, experience with BigQuery or equivalentHands on APIsProficiency with dashboarding (Looker studio/Tableau) and at least one scripting language (Python ...

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 ...

East Grinstead, United Kingdom, is seeking a Validation Engineer to ensure manufacturing processes, equipment, utilities, facilities, and systems remain qualified and compliant with GMP and quality requirements. You will prepare and maintain validation documentation, collaborate with Manufacturing, Engineering, Quality, and Regulatory Affairs, and support audits while contributing to product quality ...

manufacturing processes, equipment, and systems validated and compliant. The role emphasizes quality, regulatory compliance, and reliability while collaborating with cross-functional teams in a GMP environment. The engineer will plan, execute, and maintain validation docs, support qualification activities, perform risk and impact assessments, and assist audits and inspections to continuously ...

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 ...