101 to 125 of 137 Permanent GMP Jobs

architectures supporting business- critical production systems. Develop target-state architectures and migration strategies for large-scale technology modernisation initiatives. Ensure solutions comply with GMP/GxP requirements, validation standards, cybersecurity frameworks, and industry best practices. Experience required Extensive experience as a Solutions Architect, Enterprise Architect, or Technical Architect within regulated … environments, including industrial systems, plant infrastructure, and manufacturing technology. Proven experience delivering complex IT infrastructure transformation and migration programmes. Significant cybersecurity experience within GMP/GxP-regulated environments. #J-18808-Ljbffr ...

This job is with Organon, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Job Description Kickstart Your Career in ...

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 ...

computer systems, processing warehouse transactions, writing professional emails, organising documentation and ensuring stock and warehouse records are accurate. Pharmaceutical experience would be preferred, especially GMP or GDP knowledge, but this is not essential. Strong SAP, ERP, warehouse administration and computer skills are the key requirements. The Role As a Warehouse … emails and communicating clearly with internal and external contacts Maintaining high levels of accuracy, organisation and traceability across warehouse documentation Working in line with GMP, GDP and pharmaceutical compliance standards where required What Were Looking For We are looking for candidates who: Have previous experience in warehouse administration, logistics, distribution ...

computer systems, processing warehouse transactions, writing professional emails, organising documentation and ensuring stock and warehouse records are accurate. Pharmaceutical experience would be preferred, especially GMP or GDP knowledge, but this is not essential. Strong SAP, ERP, warehouse administration and computer skills are the key requirements. The Role As a Warehouse … emails and communicating clearly with internal and external contacts Maintaining high levels of accuracy, organisation and traceability across warehouse documentation Working in line with GMP, GDP and pharmaceutical compliance standards where required What Were Looking For We are looking for candidates who: Have previous experience in warehouse administration, logistics, distribution ...

pharmacy production, study readiness and the safe handling of investigational products and materials. Use, check and maintain pharmacy equipment in line with MHRA and GMP requirements, ensuring it remains fit for purpose and ready for clinical research activity. Monitor storage and environmental conditions for investigational products and materials, protecting product … responsibilities, final release activities, or aseptic equipment management. Investigational medicinal products handling: receipt, preparation, dispensing, accountability, storage, reconciliation, or other clinical trial pharmacy activities. GMP-regulated environments: experience gained through hospital aseptic units, clinical research facilities, manufacturing, preparation activities, or quality-driven pharmacy services. You have developed strong professional judgement ...

materials and customer communications Support commercial growth by identifying sales opportunities and maintaining strong customer relationships Ensure all activities are conducted in accordance with GMP, GDP, and applicable regulatory requirements. YOUR COMPETENCIES Bachelor's degree in Clinical Laboratory Sciences or equivalent Minimum 3 years' work experience as a laboratory technician … autoimmunity testing with expertise in IFA testing Experience and/or certification in regulatory environments such as CLIA, HIPAA, Safe-Harbor, GMP High degree of technical competence & confidence Strong customer-facing and relationship-building skills, with a consultative approach focused on delivering an excellent customer experience Excellent analytical and troubleshooting ...

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 ...

AliveDx in Penicuik, Scotland seeks a Technology Transfer Scientist to bridge R&D and Manufacturing, leading transfer activities and ensuring GMP-compliant implementation of new products and processes. You will coordinate validation programs, develop transfer strategies, and provide technical guidance across teams, while maintaining project timelines and contributing to continuous ...

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 ...

Eblex Group is supporting a growing biotechnology company with an expanding clinical pipeline in the search for a Director Clinical Quality Assurance with GMP exposure. This broad QA role sits within a lean biotech environment and works closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations ...

critical production systems. The role is remote with an initial 6-month contract for a high-impact life sciences programme, requiring extensive experience in GMP/GxP and cybersecurity within #J-18808-Ljbffr ...

team in Shawfair. You will supervise a small team handling CSV for facilities and software, ensuring milestones are met and evidence is complete for GMP audits. You will prepare and approve validation documents, coordinate with clients, and provide SME input across the business. A life sciences or CS degree supports ...

Specialist to deliver data services to our clients, which include data and benefit audits, preparing data strategies and plans, undertaking various pension rectifications including GMP rectification and equalisation. While we continue to help clients meet their GMP objectives, the data challenges our clients face are becoming more diverse which gives ...

modelling tool that feeds into our pensions actuarial and administration systems: pension scheme cashflow and liability modelling, online transfer values, benefit rectification and GMP equalisation projects; and pensions administration benefit calculations, including those shown online to members. The CALM team have varying balances of skills and experience levels across pensions … would ideally see a good working knowledge of areas such as: First principles of technical defined benefit pension calculations, including (for example): anti-franking, GMP conversion, retirement options (eg bridge pensions, pension increase exchanges, etc), pensions tax limits, etc. GMP equalisation methodologies. Comfortable with/the drive to become comfortable ...

Commercial Director in the commercial management of major CSA capital work packages from procurement through to final account. Support and, where appropriate, lead GMP development, negotiation and conversion into agreed package values. Prepare and review valuations, payment recommendations and change control. Contribute to cost reports, forecasts, CVRs and executive-level … successful candidate will ideally have: Significant experience in cost or commercial management on major capital projects. Strong post-contract cost management experience. Experience with GMP procurement, development and negotiation. Working knowledge of FIDIC contracts and contract administration. Strong experience in change control, variations and commercial management. Experience managing valuations ...

play a key role in data preparation in advance of transactions (e.g. buy‐ins); 2) conduct data audits, benefit audits and calculations; 3) undertake GMP projects. For this reason, prior GMP experience is essential. You will also have a good understanding of the technical aspects of defined benefit pensions, with ...

STEMCELL Technologies Inc., Cambridge-based, seeks a Senior Quality Engineer to support GMP cell and gene therapy product lifecycle from development through manufacturing. You will lead design control, risk management, and QA activities, aligning documentation, tests, and audits with ISO and CFR standards. The role emphasizes cross-functional collaboration with ...

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 ...

Onyx-Conseil in Stevenage offers a hybrid IT Director role to shape the IT strategy and governance for a GMP-regulated environment. The position leads external and internal customers, directs a 15-person IT team, and partners with senior leaders to enable clinical, regulatory and manufacturing workflows. You will drive ...

dedicated Quality Analyst to support the digital transformation journey of a manufacturing site, focusing on implementing and maintaining IT systems that align with GMP regulations. This role will primarily involve working with Quality Systems such as LIMS, CDS, and other QC equipment applications, while also supporting broader manufacturing IT needs. ...

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 ...

reviews for equipment, facilities, utilities, processes, cleaning validation, analytical methods and computerised systems. Role involves planning, coordinating and delivering validation activities, ensuring regulatory compliance (GMP, MHRA, EU and FDA), and supporting investigations, audits and continuous #J-18808-Ljbffr ...

Accord Healthcare Europe is seeking a suitably skilled Calibration/Instrumentation Engineer to ensure calibration systems operate to GMP, SOPs and regulatory standards. You will troubleshoot, calibrate, repair, and install equipment, while supporting the site’s electrical infrastructure and audit readiness. The role requires ONC level or equivalent in Electrical ...