1 to 25 of 448 Pharmaceutical Jobs in the UK excluding London

leads and inspires colleagues. Strong influencing and leadership skills. Understands influencing, stakeholder management and negotiation strategies. The Client is ideally seeking someone from a Pharmaceutical or Bio Science background and who understands how to work with the government and government funding. This position will manage 15 people within the IT More ❯

Experience managing data architecture, engineering, and reporting across Commercial, Medical Affairs, and Finance. Strong knowledge of enterprise and external Commercial data sources in the Pharma/BioPharma industry. Education/Qualifications: Bachelor's degree in Computer Science, Information Systems, a STEM field or equivalent. Preferably with a Master's degree More ❯

looking for BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Proficient in MS Office (Word, Excel and More ❯

closure. Educated to degree calibre in an engineering or scientific discipline we are looking for proven and highly experienced medical device, life sciences or pharmaceutical Quality Assurance, Senior Quality Assurance, Principal Quality Assurance Engineers or QA Specialists. All candidates should have strong experience leading or closely supporting ISO13485/MHRA More ❯

MBA, TOGAF, BCS) Knowledge of digital technologies like AI/ML, IoT, and blockchain within supply chains Experience in regulated industries such as FMCG, pharma, or tobacco Exposure to agile and product-centric delivery models Strong knowledge of cloud and hybrid environments (Azure preferred) Deep understanding of multiple architecture domains More ❯

an opportunity to make a long-standing and important contribution to the future state of GSK. GSK Irvine is a global site supplying Active Pharmaceutical Ingredients for key antibiotic brands in the General Medicine portfolio. The medicine produced in Irvine impacts the lives of 151 patients worldwide each year. We More ❯

engaged, and creative way with our colleagues and clients. We strive to support the transition of knowledge and capability into strategic teams. In the pharmaceutical sector, we are internationally recognised for our expertise in early-phase drug discovery, genomics, and human genetics. In late 2023, we proudly launched our new More ❯

significant majority of the below for: Significant consulting experience, client-facing stakeholder management skills, or equivalent tenure in relevant industries (FS, Insurance, Energy & Utilities, Pharma & Lifesciences etc.). Demonstratable proficiency in technology strategy and architecture having been responsible for strategic technology roadmaps and/or enterprise architecture as part of More ❯

solving skills and attention to detail Effective communication and collaboration skills Ability to work independently and as part of a team Knowledge of the Pharma or healthcare industry is a + What we offer Integration in a highly qualified, successful and ambitious team International Startup feeling in the heart of More ❯

global teams Promote quality culture across the organization Required Qualifications Bachelor's degree in Science or QA discipline (or equivalent experience) 5-10 years' pharmaceutical industry experience in QA roles Advanced experience implementing IT PQS systems (particularly Veeva Vault) Documentation management expertise Essential Skills Excellent documentation writing capabilities Strong communication More ❯

specialization) with 3-5 years of industry experience. Certified in IEMA Environmental Management or equivalent. Experience in FMCG, preferably in high care environments like pharmaceutical, healthcare, or food. Knowledge of UK regulatory standards and ISO standards (ISO14001, OHSAS18001, ISO9001). Achievement-oriented, resilient, and able to work under pressure. Strong More ❯

deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis and machine learning. Experience working with high More ❯

track record of timely execution of priorities, creation of realistic visions, cross-functional stakeholder management, and streamlining manual processes into automated flows. Familiarity with pharmaceutical compliance risks or compliance considerations for stakeholder engagements is a plus. Fluency in SQL, PowerQuery, star-schemas, DAX, or similar coding languages and approaches is More ❯

SAP IC Hub knowledge. Knowledge of legal/government reporting regulations. Serialization experience. Experience with systems/landscapes specific to the Life Sciences or Pharmaceutical industry. Knowledge in Plasma specific processes/fractionation. Experience in Computer System Validation (legal requirements and practical knowledge). Exposure to S4HANA Public Cloud or More ❯

or a related field (or equivalent practical experience). 5 years + of experience in quality management in industries such as semiconductor, automotive, aerospace, pharmaceutical/medical, and electronics industries with similar quality standards. Comprehensive knowledge of quality management systems (e.g., ISO 9001, IATF 16949 or similar). Experience in More ❯

relevant professional experience. Qualification: Extensive experience in delivering Enterprise level SAP Finance and controlling solutions including S/4 experience, with strong preference for pharmaceutical industry experience. Proficiency in SAP Cost Accounting configuration and testing in all major areas. Professional certifications (SAP FICO, PMP, CMA, etc.) are a plus. Familiarity More ❯

more efficiently. On site we produce over 60 million respiratory inhalers each year with growing demand in future years. The site also processes Active Pharmaceutical Ingredient (API) for use both on site and other manufacturing sites in our network. CLOSING DATE for applications: Tuesday 27th of May 2025 (COB) Basic More ❯

opportunity to personally make a long standing and important contribution to the future state of GSK. GSK Irvine is a Global site supplying Active Pharmaceutical Ingredient for K ey A ntibiotic brand in General Medicine portfolio. The medicine we make in Irvine impacts the lives of 151 patients worldwide every More ❯

and NoSQL databases Degree (BSc, MSc, or PhD) in Computer Science, Engineering , or a related field Highly beneficial if you have worked within the Pharmaceutical industry along with knowledge in machine learning, AI , data engineering , or DevOps/containerization More ❯

inspection readiness and internal performance monitoring Contribute to Quality leadership team projects and initiatives to enhance overall site compliance Ideal Experience: Extensive experience in pharmaceutical QA, with a strong understanding of GMP and GDP Proven track record in managing QMS elements, including validation, documentation, and data integrity Experience supporting inspections More ❯

Profibus, Modbus, DeviceNet). Knowledge of process instrumentation and wiring would be desirable. Experience working with validated Digital Manufacturing/Automation systems in the Pharmaceutical or Food Beverage manufacturing environment. Characteristics We look for candidates who Work well as part of a team. Have excellent problem solving and diagnostic skills. More ❯

regulatory compliance projects Educated to degree calibre in an engineering or scientific discipline we are looking for an experienced medical device, life sciences or pharmaceutical Quality Assurance Engineer or Quality Assurance Specialist. Candidates should have some experience supporting ISO13485/MHRA audits, contributing to QA projects across a business and More ❯

with third party SSO providers. Experience with databases: configuration, management, and diagnosing and resolving issues. Experience in one or more of these domains: LIMS, Pharmaceutical R&D, Chromatography, Laboratory automation. Visual Studio, C#, and .NET development experience. Experience working with a global, international team. Work Environment: The position will be More ❯

process. SAP ATTP and SAP IC Hub knowledge. Understanding of legal/government reporting regulations. Experience with systems specific to the Life Sciences or Pharmaceutical industry. Knowledge of Plasma-specific processes/fractionation. Experience in Computer System Validation (legal requirements and practical knowledge). General: Career opportunities along multiple routes More ❯

SAP IC Hub knowledge. Knowledge of legal/government reporting regulations. Serialization experience. Experience with systems/landscapes specific to the Life Sciences or Pharmaceutical industry. Knowledge in Plasma specific processes/fractionation. Experience in Computer System Validation (legal requirements and practical knowledge). GENERAL Career opportunities exist along multiple More ❯