1 to 25 of 766 Pharmaceutical Jobs in the UK

applications, digital) etc. 10 - 12+ years of experience in Technology and/or Architectural consulting. Formative experiences in architecture, software engineering, data, and analytics. Pharmaceutical, Biotech or similarly regulated environment experience desirable. Must have hands-on experience in leading, managing, or overseeing core development project(s) and engineering teams. Must More ❯

product performance, roadmap, and future plans. Industry Thought Leadership: Stay abreast of industry trends, best practices, and emerging technologies in the protein design and pharma tech space. Share insights and act as a thought leader within the organization and industry events External Collaboration Leadership: Identify, initiate, and manage strategic collaborations More ❯

product performance, roadmap, and future plans. Industry Thought Leadership: Stay abreast of industry trends, best practices, and emerging technologies in the protein design and pharma tech space. Share insights and act as a thought leader within the organization and industry events External Collaboration Leadership: Identify, initiate, and manger strategic collaborations More ❯

product performance, roadmap, and future plans. Industry Thought Leadership: Stay abreast of industry trends, best practices, and emerging technologies in the protein design and pharma tech space. Share insights and act as a thought leader within the organization and industry events External Collaboration Leadership: Identify, initiate, and manger strategic collaborations 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 ❯

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 ❯

innovations, positioning them within broader industry trends to inform internal teams and external stakeholders. Lead simultaneous client facing projects across ZS Discovery to reinvent pharmaceutical discovery, elucidate complex disease biology and pioneer novel therapeutics. Provide expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics 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 ❯

Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We More ❯

clearly demonstrated. Industry/domain skills: Extensive expertise in finance, HR, sales, marketing, product lifecycle management, manufacturing and post-sales service. Medical device or pharmaceutical industry experience is preferred. Experience in and understanding of a wide variety of analytical processes (governance, measurement, etc.). Experience with agile software development. A 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 ❯

or a related field, or equivalent work experience. Strong experience in agile environments, particularly in customer-facing deployments. Knowledge or experience in Life Sciences, Pharma workflows, or GxP compliance-related activities is a plus. Competitive Salary and equity in a fast-growing company. Generous Paid Time Off (PTO) and wellness More ❯

strong background in programme and project management, stakeholder engagement, and the ability to work across multiple teams to drive successful outcomes. Experience in the pharmaceutical industry or another regulated sector would be an advantage. Responsibilities: Programme Management: Lead and manage multiple projects, ensuring alignment with strategic business goals and objectives. More ❯

solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE platform, have proven to maximize the supply chain, minimize operational costs, and ensure More ❯

years of laboratory automation experience is preferred Experience leading development and implementation of automated laboratory workflows or high-throughput methods within the biotechnology/pharmaceutical industry; this includes systems configuration, liquid handling, and method programming is required Experience designing, programming, operating, and troubleshooting end-to-end integrated automation systems, such 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 ❯

QA and QC processes alongside all QM elements in one or more of the following sectors is an advantage: Aerospace and Defence, Consumer Products, Pharma or Discrete Manufacturing. Leadership experience across small to medium-sized teams, both onshore and offshore. Commitment, flexibility, thought leadership and a hunger to develop your More ❯

job. - PM1 Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Information Technology Industries Biotechnology Research, Pharmaceutical Manufacturing, and Research Services Referrals increase your chances of interviewing at Syneos Health by 2x Sign in to set job alerts for "Project Data Manager More ❯

chat. The AI/ML Clinical Development team is responsible for creating AI/ML applications to support the development of GSK's assets (Pharma and Vaccine), from early to later-stage development, aligned with GSK's strategy of "software for every asset." Solutions range from response prediction to complex More ❯

solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE platform, have proven to maximize the supply chain, minimize operational costs, and ensure More ❯

headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. GRAIL is looking for a full-stack Senior Software Engineer to join its clinical software team based in our London office. 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 ❯

everyone individually if you are not successful. About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over More ❯