1 to 25 of 615 Pharmaceutical Jobs in England

pain, oncology, inflammation and metabolic diseases. Leveraging these skills and expertise the Company intends to develop best-in-class differentiated therapeutics and deliver superior science-driven discovery alliances with pharmaceutical and biotechnology companies. Key Responsibilities SAP Process Leadership and Design End-to-End SAP Solutions: Lead the design, implementation, and support of SAP Manufacturing (PP-PI) and Quality (QM) processes … testing, troubleshooting, and continuous improvement initiatives. Strong analytical and problem-solving capabilities, with a demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions. Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments. Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards. Bachelor's degree in Information Technology, Engineering, Business, or … The Company's multimodality platform comprises a unique combination of innovative technologies, data and science for the discovery, development, and production of first-in-class and best-in-class pharmaceutical products. Evotec leverages this "Data-driven R&D Autobahn to Cures" for proprietary projects and within a network of partners including all Top 20 Pharma and over 800 biotechnology companies More ❯

have are delighted to be recruiting for a Senior Clinical Data Analyst to join our client, an SME specialising in the development of software products and eCOA for the pharmaceutical and healthcare sectors. As the business continues to grow, this is an excellent opportunity to play a key and leading role within study teams across a number of client phase More ❯

platforms are fundamentally reshaping how organisations discover, develop, and bring therapies to patients. At Accenture, we sit at the heart of this evolution-partnering with the world's leading pharmaceutical and biotech companies to reimagine R&D for a more predictive, efficient, and patient-focused future. Our Data & AI R&D team within the Strategy & Consulting practice is driving this … You Will: Deliver client-facing work that applies data and AI solutions to improve drug development and clinical trial performance Leverage your understanding of clinical development, either from within pharma or consulting, to inform strategic problem-solving and solution design Contribute to projects involving trial scenario simulations, protocol optimization, recruitment forecasting, and digital twin models Work closely with multidisciplinary teams More ❯

platforms are fundamentally reshaping how organisations discover, develop, and bring therapies to patients. At Accenture, we sit at the heart of this evolution-partnering with the world's leading pharmaceutical and biotech companies to reimagine R&D for a more predictive, efficient, and patient-focused future. Our Data & AI R&D team within the Strategy & Consulting practice is driving this … You Will: Deliver client-facing work that applies data and AI solutions to improve drug development and clinical trial performance Leverage your understanding of clinical development, either from within pharma or consulting, to inform strategic problem-solving and solution design Contribute to projects involving trial scenario simulations, protocol optimization, recruitment forecasting, and digital twin models Work closely with multidisciplinary teams More ❯

platforms are fundamentally reshaping how organisations discover, develop, and bring therapies to patients. At Accenture, we sit at the heart of this evolution-partnering with the world's leading pharmaceutical and biotech companies to reimagine R&D for a more predictive, efficient, and patient-focused future. Our Data & AI R&D team within the Strategy & Consulting practice is driving this … You Will: Deliver client-facing work that applies data and AI solutions to improve drug development and clinical trial performance Leverage your understanding of clinical development, either from within pharma or consulting, to inform strategic problem-solving and solution design Contribute to projects involving trial scenario simulations, protocol optimization, recruitment forecasting, and digital twin models Work closely with multidisciplinary teams More ❯

pain, oncology, inflammation and metabolic diseases. Leveraging these skills and expertise the Company intends to develop best-in-class differentiated therapeutics and deliver superior science-driven discovery alliances with pharmaceutical and biotechnology companies. Key Responsibilities SAP Process Leadership and Design End-to-End SAP Solutions: Lead the design, implementation, and support of SAP Manufacturing (PP-PI) and Quality (QM) processes … testing, troubleshooting, and continuous improvement initiatives. Strong analytical and problem-solving capabilities, with a demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions. Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments. Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards. Bachelor's degree in Information Technology, Engineering, Business, or More ❯

in Data Science, Statistics, Computer Science, Business Analytics, or a related field. Advanced degree preferred. Demonstrated experience in data analytics, business intelligence, or a related field, preferably within the pharmaceutical or healthcare industry. Strong analytical and problem-solving skills. Proficiency in data analytics tools and software (e.g., SQL, Python, R, Tableau, Power BI). Excellent communication and presentation skills. Ability … Until the 39 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in More ❯

and continuous improvement initiatives. Strong analytical and problem-solving capabilities, with a demonstrated ability to translate complex business requirements into efficient, integrated SAP solutions. Industry Insight: Experience working within pharmaceutical, biotech, or similarly regulated manufacturing environments. Familiarity with GxP protocols, FDA regulatory compliance, ISO standards, and other pertinent quality assurance standards. Educational Background & Certifications: Bachelor's degree in Information Technology More ❯

edge digital solutions including Manufacturing Execution System (MES) solutions for the Life Sciences industry. We are a leading partner of Tulip Interfaces having deployed Tulip successfully for top 10 Pharma to more than 30 sites worldwide. We are committed to delivering innovative technology solutions that enhance productivity, ensure regulatory compliance, and drive digital transformation for our clients. Position Overview: We … tools, is an advantage but not essential as extensive technical training will be provided. Proven experience in leading complex MES projects from concept to deployment. Knowledge and understanding of Pharma and Biotech industry & processes. Familiarity with GMP, FDA 21 CFR Part 11, GAMP5, and other relevant regulatory requirements. Excellent problem-solving, communication, and interpersonal skills. Ability to travel as required More ❯

mentor team of 6-10 integration developers while collaborating with functional consultants and business stakeholders •? Ensure regulatory compliance for all integrations including validation documentation, audit support, and adherence to pharmaceutical industry standards •? Develop APIs and custom connectors for seamless connectivity with third-party life sciences applications (CTMS, eTMF, clinical trial systems) •? Implement comprehensive testing strategies including unit, integration, and end … Bachelor's degree in Computer Science, IT, or Engineering; SAP certifications preferred •? Strong leadership and communication skills with ability to present technical solutions to business leadership Preferred: SAP certifications, pharmaceutical supply chain/serialization knowledge, DevOps/CI-CD experience, Master Data Governance (MDG) expertise Location – Luton or Macclesfield More ❯

related experience, will be considered sufficient for an individual to meet the requirements of the role. Required Skills/Experience Process Automation : Experience in automation within the biopharmaceutical or pharmaceutical industry or another industry. GMP experience required. Good understanding of the biopharmaceutical/pharmaceutical development process. Expertise in commissioning and validation of automation systems. Understanding of device networking and communication … and administration. Preferred technologies: SAP, Labware, LIMS, ELN, OpenLab, Empower, OneCDS, Hamilton, Beckman Coulter, Thermo Scientific, automated liquid handlers. Analytical Techniques and Automation : Experience developing and executing biopharmaceutical/pharmaceutical assays/methods and operating/troubleshooting laboratory equipment. Familiarity with current industry trends in lab automation. Experience with automated/automating data flows from testing design through analytical equipment More ❯

in a safety-first approach. Skills & Experience: 5+ years' experience working in a manufacturing industry or similar role. Educated to degree level or equivalent in a Manufacturing, Chemical Engineering, Pharmaceutical Engineering, or related field. Experience of any of the following - GMP working environment, Validation, Project management, ISO 9001 and working within a QMS. Knowledge of lean manufacturing principles, Six Sigma … or other continuous improvement methodologies is a plus. Good understanding of the pharmaceutical industry standards and regulatory requirements (cGMP, FDA, EMA) is an advantage. Experience in managing multiple projects at the same time. Computer literate, familiar with Microsoft Word and Excel Key Capabilities: Good organisational, interpersonal, and time management skills. Enthusiastic, flexible, conscientious and proactive in approach. Take a positive More ❯

requirements. Qualified EU/UK based candidates are encouraged to apply. What You'll Do Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechs Lead the solution design for implementation and use of the Vault Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) Lead configuration requirements workshops … other regulatory information management or submission publishing systems, etc. Consulting experience, working with a major system integrator or software vendor Regulatory Affairs, Regulatory Operations or Pharmacovigilance background Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content PMP certification Execution experience with Agile methodology and/or ACP Certification Life Science, computer science, or More ❯

with GMP and minimizing disruptions to project timelines and costs. About you Experience : Proven track record of managing complex manufacturing systems involving automation, robotics, and advanced technologies, in the pharmaceutical sector. Technical Skills : Proficiency in Process Control Systems, SCADA, PLCs, and other automation technologies, with the ability to design and implement robust system integration architectures. Education : A degree in Engineering … Automation, Computer Science, Biotechnology, Pharmaceutical Sciences, or a related field. Soft Skills : Strong analytical and problem-solving skills, effective communication with stakeholders, leadership and cross-functional teams. Languages : Proficiency in English is essential; additional language skills are a plus. Why choose us? At Sanofi, we believe in continuous learning and development. We encourage innovative thinking and welcome fresh ideas for More ❯

stakeholder management. Demonstrated experience with Azure stack (databricks, AMLS, etc.) Knowledge of the data landscape in healthcare (EHR, claims data, real world data, HEOR data) Experience in healthcare/pharmaceutical industry Experience in sales and digital marketing analytics Closing Date for Applications 18th July 2025 (COB) Please take a copy of the Job Description, as this will not be available … Until the 39 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in More ❯

or similar) Demonstrated experience in product ownership and stakeholder management. Knowledge of the data landscape in healthcare (EHR, claims data, real world data, HEOR data) Experience in healthcare/pharmaceutical industry Experience in Medical affairs and digital marketing analytics Why ViiV? ViiV Healthcare is a global specialty HIV company, the only company that is 100% focused on researching and delivering … Until the 39 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in More ❯

or similar) Demonstrated experience in product ownership and stakeholder management. Knowledge of the data landscape in healthcare (EHR, claims data, real world data, HEOR data) Experience in healthcare/pharmaceutical industry Experience in sales and digital marketing analytics Why ViiV? ViiV Healthcare is a global specialty HIV company, the only company that is 100% focused on researching and delivering new … Until the 39 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV. We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At ViiV Healthcare, we do things differently. Born out of a partnership between GSK and Pfizer in More ❯

We have an exciting opportunity for a Business Analyst Graduate to work for our global pharmaceutical client located in Moorgate, London. This role will support our efforts in forecasting, market research, analytics, and insights, with a specific focus on customer engagement. The successful candidate will play a key role in deploying a regional Core Europe and Canada (CER) tool into More ❯

ERP systems— particularly Microsoft Dynamics 365 Finance & Operations (D365 F&O). Proven expertise in Supply Chain and Manufacturing modules (inventory, procurement, production, demand planning). Experience in the pharmaceutical industry or a similarly regulated, GxP-compliant environment. Strong understanding of ERP best practices, master data management, and process transformation in global organizations. Skilled in gathering requirements, facilitating workshops, and More ❯

We have an exciting opportunity for a Business Analyst Graduate to work for our global pharmaceutical client located in Moorgate, London. This role will support our efforts in forecasting, market research, analytics, and insights, with a specific focus on customer engagement. The successful candidate will play a key role in deploying a regional Core Europe and Canada (CER) tool into More ❯

insights based on ZS-driven 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, bulk or single cell RNA More ❯

s degree in Automation Engineering, Mechatronics, Electrical Engineering, Computer Science, or related field. Experience in designing and implementing automation solutions, ideally in R&D or manufacturing environments (food or pharma experience is a plus). Proven experience in writing User Requirements Specifications (URS) and effectively collaborating with external vendors, integrators, or partners throughout the project lifecycle. Proficiency in robotic systems More ❯

projects About you: Independent, self-motivated & results driven individual Willingness & ability to acquire quickly new technical skills & business principles Ability for Critical Thinking and Logical Reasoning Good understanding of pharmaceutical research and drug Discovery & development processes and biologics workflows(preferred, not required) Required Education/Experience: Bachelor of Science in computer science, life science or equivalent industry experience 2+ years … of relevant technical experience including (but not limited to); biotech/pharmaceutical company or an automation provider. Experience with scientific instrumentation (preferred) About Zifo: CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit … of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team's knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies. We look for Science - Biotechnology More ❯

skills to achieve our goals: Degree in a Science/Engineering related discipline such as Automation, Control, Electrical or Mechatronic. Six Sigma and Lean Manufacturing experience gained from the pharmaceutical industry.; Black Belt or Green Belt desirable. Technical expertise in several scientific and engineering automation areas including ISA standards (e.g. S88, S95), P&ID nomenclature, Automation architecture, instrumentation and electrical … it would be a plus: MEng/MSc in a Science or Engineering related discipline such as Automation, Control, Electrical or Mechatronic. A sound scientific and engineering understanding of pharmaceutical secondary processing. Good knowledge of IT architecture management, data warehousing, virtualization & implementation processes. Practical knowledge of Cybersecurity within an OT space. Demonstrated project management skills. Working knowledge and understanding of … EHS Practices and regulations with respect to the installation of automated plant. A good appreciation of FDA PAT initiatives and the impact on the Pharma industry. Proven track record in providing automation support and maintenance for instrumentation, automation and controls. Closing Date for Applications 16th July 2025 (EOD) Please take a copy of the Job Description, as this will not More ❯

and One STADA to achieve ambitious goals and shape the successful future of STADA. Britannia Pharmaceuticals , part of the STADA Arzneimittel AG group of companies, is a UK based pharmaceutical company specialising in the neurology market. Britannia focuses on innovative products for chronic and serious medical conditions, and in particular, the treatment of Parkinson's disease. We are highly committed More ❯