1 to 25 of 437 Pharmaceutical Jobs in the UK excluding London

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 ❯

and Data Orchestration Software) to enhance accessibility and user experience for scientists across RTech. This position offers an exciting opportunity to make a significant impact on the future of pharmaceutical research at GSK. This role will report to the Head of RTech Automation UK/US and will join the new RTech Automation Leadership Team to shape our vision and … degree in Computer Science, Engineering, Life Sciences, or a relevant scientific subject area; advanced degree preferred. A minimum of 8 years of experience in digital automation, preferably within the pharmaceutical or biotechnology industry. Proven track record of leading digital transformation projects and implementing automation solutions in a research or laboratory setting. Experience with laboratory information management systems (LIMS), electronic lab … data analytics. Track record of team leadership, with a focus on fostering collaboration and innovation. Preferred Skills : Knowledge of regulatory requirements and industry standards related to digital automation in pharmaceutical research. Excellent project management skills with the ability to manage multiple initiatives simultaneously. Strong problem-solving skills and the ability to think strategically and creatively. Excellent communication and interpersonal skills More ❯

infrastructure requirements Experience supporting bioinformatics workflows Familiarity with container technologies (Docker, Kubernetes) Experience with infrastructure automation tools Understanding of scientific computing software and frameworks Previous experience in biotech or pharmaceutical industries Experience with cloud platforms (AWS, Azure) ITIL certification Security certifications (CISSP, CISM, or similar) Experience with GxP compliance Experience with pharmaceutical industry regulations Previous experience managing technical debt in 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 ❯

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 ❯

projects and priorities simultaneously. Previous experience in a management or leadership role with line responsibilities Preferred Qualifications : Deep knowledge of safety requirements and industry standards related to automation in pharmaceutical research. Outstanding analytical and problem-solving skills, with the ability to quickly address and resolve technical challenges. Excellent communication and interpersonal skills, with the ability to effectively convey technical concepts … and resolve technical challenges. Excellent communication and interpersonal skills, with the ability to effectively convey technical concepts to a diverse set of stakeholders. If you are passionate about advancing pharmaceutical research through innovative automation platforms, we invite you to join our team at GSK. Apply now and be part of a company that is dedicated to improving the quality of 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 ❯

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 ❯

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 ❯

achieved. The role operates as part of the site's Capital Engineering organization with responsibility for project delivery for the site's capital project portfolio. Project examples include new pharmaceutical production equipment (eg; tablet presses, packing equipment or bespoke blending and filling equipment) as well as covering a range of site infrastructure (including warehousing, boiler systems, etc) and critical utilities … demonstrate strong partnering skills (both internal customers and external suppliers and contractors). You will also have strong knowledge and understanding of scientific/technical design and operation of pharmaceutical manufacturing facilities. About Ware Manufacturing Site: Medicines at Ware are presented as either Respiratory devices or in Oral Solid Dose form, and the site has circa 1,500 highly-motivated More ❯

research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an More ❯

research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an 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 ❯

Requirements: (1) Demonstrated ability with software development lifecycle (SDLC) gained through three (3) years of work experience; 2) Demonstrated ability working with IT Operations for business users in the pharmaceutical or life science industries gained through three (3) years of work experience; and 3) Demonstrated ability working with Enterprise Applications, specifically Veeva Vault, Workday, Concur, SAP, JIRA, Oracle, ComplianceWire or More ❯

BS, BA) or equivalent professional experience is required, preferably in Health Sciences or Data Sciences. Advanced degrees preferred (e.g., Masters, PhD). Minimum 8-12 years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry! Knowledge of trial site operations and study execution Strong knowledge of regulatory guidelines (e.g., ICH-GCP). Demonstrated strong understanding of More ❯

opportunities within their defined geographic territory, focusing on selling development and clinical to commercial manufacturing services for Gene and Cell Therapy products to customers across the whole of the Pharmaceutical and Biotechnology industries As a Business Development Director you will join our dynamic Business Development Teams for Europe and North America and your primary role is to evaluate and assess … contract manufacturing opportunities with our bio pharma customers. You will also align internal capabilities and services with the customers' outsourcing needs for Cell and Gene Therapy. You will be responsible for developing current and new business opportunities in UK/Ireland and the Nordics. Main Responsabilities: Achieve annual sales, revenue, and funnel targets to ensure continued growth. Develop and maintain … us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per More ❯

of equipment, process, utilities, facilities, computer systems, etc. Essential Requirements: Degree or equivalent qualification in a life science or similar subject Extensive recent experience of QA leadership in a Pharma/CMO company. Proven track record in supporting QP release. Excellent knowledge of global regulations, and experience of dealing with MHRA. Good communication skills internally and in a client facing … of equipment, process, utilities, facilities, computer systems, etc. Essential Requirements: Degree or equivalent qualification in a life science or similar subject Extensive recent experience of QA leadership in a Pharma/CMO company. Proven track record in supporting QP release. Excellent knowledge of global regulations, and experience of dealing with MHRA. Good communication skills internally and in a client facing More ❯

Salesforce Administrator Locations UK Type home-based Position type Full-time, permanent role About Labcorp: We are a global leader in innovative and comprehensive laboratory services, helping doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. With over 60,000 employees, our cutting-edge diagnostics and drug development capabilities address major health challenges, accelerate healthcare breakthroughs, and … policies. Training & development: Access various training formats to grow your career and develop a global mindset. Why us: Labcorp is a leader in diagnostics and drug development, supporting global pharmaceutical advancements. Top provider in clinical trial data and early-phase solutions. First to receive FDA approval for at-home COVID-19 testing kits. Recognized as one of Forbes' World's More ❯

to £40k (depending on experience) Sonrai is a Belfast-based AI data discovery company on a mission to help save patient lives through AI technology. We enable Biotech and Pharma companies to reduce the cost, time, and risk from early discovery to clinical trials, accelerate drug, biomarker, and diagnostics, maintain a secure and compliant Trusted Research Environment, and effectively and … our strategy. It's a great time to be joining Sonrai; over the past two years, we have: Successfully grown our customer base across a range of biotech and pharma organisations globally Grown our team to 35+ and won multiple awards Opportunity & Responsibilities The Customer Success Manager will work closely with the Director of Customer Success and the wider Sonrai More ❯