126 to 150 of 247 Pharmaceutical Jobs in the UK excluding London

Data Programme Manager - Pharma - £800 Per Day - Outside IR35 A leading pharmaceutical business is seeking a highly motivated Data Programme Manager to drive complex, cross-functional data initiatives with a strong emphasis on AI and enterprise data platforms. This role offers the opportunity to shape how the organisation leverages advanced technologies - including Oracle solutions - to accelerate drug discovery, improve clinical … technology partners to align business needs with data, AI, and Oracle platform opportunities. Data Strategy & Architecture: Ensures adherence to data governance frameworks, FAIR principles (Findable, Accessible, Interoperable, Reusable), and pharma regulatory standards (e.g., GxP). Change Management: Champions a culture of data and AI adoption across the business, ensuring teams are empowered to use new tools and insights effectively. Vendor … Ethics: Ensures responsible and ethical use of AI, with attention to patient privacy, data security, and industry regulations. Skills & Experience Proven track record in programme or project management within pharma, biotech, or life sciences. Strong expertise with Oracle databases, data warehouses, and cloud platforms , with experience in large-scale data integration and optimisation. Experience delivering AI/ML initiatives from More ❯

Role: -QA Manager-Pharma Biotech (Sterile) Location: -Alderley Edge - onsite only Salary: - Competitive salary (DOE) Hours: Days (Monday - Friday) 40 hours per week Benefits: 25 days holiday + BH, private medical care, share options scheme &company pension Russell Taylor Group have a fantastic opportunity for a QA Manager with sterile experience to join a continually growing SME in Cheshire. Our … one to one appraisals and performance reviews. Provide monthly KPI metrics in relation to quality. Requirements: Degree in Life Sciences or related discipline. Proven experience in QA management within pharmaceutical, biotech, or medical manufacturing- experience of directly managing individuals is essential for this role. Previous direct experience of CAPA, Change control, root cause analysis & deviations Experience in a sterile environment. More ❯

enabling continuous improvement. Job Description: Join us in supporting the creation and deployment of next generation digital manufacturing solutions using the Tulip (https://tulip.co/) platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the way life sciences manufacturers digitally transform using the very latest software tooling and methodologies. Openness to working in new ways with … a flexible and creative mindset is key, as for most Pharma IT professionals this will be more agile and fast paced, and for people from non-regulated backgrounds work may require more structure and quality management. Work is delivered in tight collaborative teams with colleagues and customers, so a collaborative attitude and strong communications skills are essential. We are delivering … years’ experience in managing some IT system/software development and/or implementation projects. Good understanding of the manufacturing process execution, with a strong preference for experience in pharmaceutical manufacturing. Knowledge of software delivery projects Experience of managing multiple projects at a time, ranging from small to large scale and critical systems. Expertise in typical project management tools for 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 ❯

Piramal Pharma is a world-leading developer and manufacturer of high-quality biological reagents and is seeking a Quality Assurance officer to join their growing team in our QA department in Grangemouth. The Quality Assurance officer will act as the Quality Assurance representative for campaign projects, ensuring accuracy and compliance of procedures, quality management system records, manufacturing batch records and More ❯

data to inform study design decisions. The Informatics team utilizes informatics principles and techniques to architect, mine, analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies. The team is seeking an experienced … of more junior team members. 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 leverage local regulatory and therapeutic More ❯

What's in it for you At Booker, along with being a great place to work and giving you an opportunity to get on in your career, we also offer the following fantastic package of benefits: A Booker colleague card More ❯

Systems Validation (CSV) Specialist , you will be required to support the validation and lifecycle management of both custom-built and commercial off-the-shelf (COTS) systems used throughout our pharmaceutical operations. This role is essential to ensuring compliance with GAMP 5 guidelines and global regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11), while also supporting a company … in this role, you should be able to demonstrate: Bachelor's degree in a scientific, engineering, or IT-related field. Minimum of 3 years’ experience in CSV within the pharmaceutical or life sciences industry. Strong understanding of GAMP 5, data integrity requirements, and applicable regulatory frameworks. Demonstrated experience with both bespoke and COTS systems across a range of GxP areas 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 ❯

What's in it for you At Booker, along with being a great place to work and giving you an opportunity to get on in your career, we also offer the following fantastic package of benefits: A Booker colleague card More ❯

Senior Software Engineer Department: Engineering Employment Type: Full Time Location: Manchester, UK Description Interact provides enterprise-grade intranet software that connects over three million employees to leading global names like Levi's, Domino's, Teva Pharmaceuticals, and Technicolor. Our team More ❯

What's in it for you At Booker, along with being a great place to work and giving you an opportunity to get on in your career, we also offer the following fantastic package of benefits: A Booker colleague card More ❯

Data Engineer - AI/ML | Leading Pharma | London (Hybrid) My client a leading pharmaceutical company is looking for a Data Engineer who thrives on solving complex challenges and building scalable data solutions that power scientific innovation. Key Responsibilities Build and maintain data pipelines using Python, Spark, SQL, BigQuery , and Google Cloud Collaborate with scientists to meet research data needs Ensure More ❯

initiative to solve problems. Strong interpersonal and communication skills, with fluency in English (written and spoken). A proactive, “team-first” attitude and commitment to continuous improvement. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. More ❯

initiative to solve problems. Strong interpersonal and communication skills, with fluency in English (written and spoken). A proactive, “team-first” attitude and commitment to continuous improvement. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. More ❯

candidates) ?????? Client: Viatris (Confidential) ?? Eligibility: Open to European Citizens , Irish Nationals , or Stamp 4 holders (with minimum 12-month IRP validity) About the Client Our client, a leading global pharmaceutical organization , is seeking experienced SAP serialization professionals to join their Dublin-based team. These roles will play a critical part in ensuring global compliance, product traceability, and efficient serialization operations … within their enterprise systems. Position 1: SAP ATTP (Advanced Track and Trace for Pharmaceuticals) Functional Lead Experience Required 10+ years of overall SAP experience Minimum 2 end-to-end pharma serialization implementations using SAP ATTP (Mandatory) Key Responsibilities Lead SAP ATTP (S/4HANA) implementation for pharmaceutical serialization. Perform gap analysis in enterprise serialization systems. Prepare functional specifications, test scripts … business SMEs for training, documentation, and change management . Support integration with other SAP modules (MM, SD, PP, EWM) and external systems (Trackwise). Required Skills Deep understanding of pharma serialization and packaging processes . Strong hands-on experience in SAP ATTP S/4HANA (integrations, upgrades, AIF configuration, rules framework). Experience in divestiture or integration projects . Excellent More ❯

candidates) ?????? Client: Viatris (Confidential) ?? Eligibility: Open to European Citizens , Irish Nationals , or Stamp 4 holders (with minimum 12-month IRP validity) About the Client Our client, a leading global pharmaceutical organization , is seeking experienced SAP serialization professionals to join their Dublin-based team. These roles will play a critical part in ensuring global compliance, product traceability, and efficient serialization operations … within their enterprise systems. Position 1: SAP ATTP (Advanced Track and Trace for Pharmaceuticals) Functional Lead Experience Required 10+ years of overall SAP experience Minimum 2 end-to-end pharma serialization implementations using SAP ATTP (Mandatory) Key Responsibilities Lead SAP ATTP (S/4HANA) implementation for pharmaceutical serialization. Perform gap analysis in enterprise serialization systems. Prepare functional specifications, test scripts … business SMEs for training, documentation, and change management . Support integration with other SAP modules (MM, SD, PP, EWM) and external systems (Trackwise). Required Skills Deep understanding of pharma serialization and packaging processes . Strong hands-on experience in SAP ATTP S/4HANA (integrations, upgrades, AIF configuration, rules framework). Experience in divestiture or integration projects . Excellent More ❯

product execution to deliver software that solves real chemical safety assessment problems. You will own outcomes across discovery, delivery, and iteration, ensuring our solutions reflect real scientific workflows in pharmaceutical and chemical domains and create measurable value for members and regulators. You will collaborate daily with scientists, software developers, application scientists, and member stakeholders to shape strategy, prioritise the backlog … impact and iterate to maximise value. Discovery and scientific design Partner with application and research scientists to map end-to-end scientific workflows, data needs, and decision points across pharma and chemical safety. Translate scientific problems into well shaped opportunities, features, and testable hypotheses – with clear success metrics and acceptance criteria. Ensure designs uphold scientific integrity, traceability, and explainability, and … facilitate trade-offs, and keep decisions visible. Contribute to product management standards and mentoring across teams. About you Essential Degree or higher in a relevant scientific field – e.g., chemistry, pharmaceutical sciences, toxicology, metabolism, degradation, or related disciplines. Demonstrated Product Owner or closely related product role experience in scientific or deeply technical software. Strong Agile skills – backlog management and prioritisation, user More ❯

product execution to deliver software that solves real chemical safety assessment problems. You will own outcomes across discovery, delivery, and iteration, ensuring our solutions reflect real scientific workflows in pharmaceutical and chemical domains and create measurable value for members and regulators. You will collaborate daily with scientists, software developers, application scientists, and member stakeholders to shape strategy, prioritise the backlog … impact and iterate to maximise value. Discovery and scientific design Partner with application and research scientists to map end-to-end scientific workflows, data needs, and decision points across pharma and chemical safety. Translate scientific problems into well shaped opportunities, features, and testable hypotheses – with clear success metrics and acceptance criteria. Ensure designs uphold scientific integrity, traceability, and explainability, and … facilitate trade-offs, and keep decisions visible. Contribute to product management standards and mentoring across teams. About you Essential Degree or higher in a relevant scientific field – e.g., chemistry, pharmaceutical sciences, toxicology, metabolism, degradation, or related disciplines. Demonstrated Product Owner or closely related product role experience in scientific or deeply technical software. Strong Agile skills – backlog management and prioritisation, user More ❯

Computer System Validation (CSV) Engineer 📍 Location: Surrey | 💼 Contract | 🏭 Pharmaceutical Manufacturing We are on the hunt for Computer System Validation (CSV) Engineer to join our client for an exciting capital project involving a new production line. This role is critical in ensuring that all computerised systems are validated, compliant, and operate reliably in accordance with GxP and industry regulations. You will … What You Need: Degree in Science, Engineering, IT or related discipline, or equivalent practical experience. Strong knowledge of cGMP, GAMP 5 and relevant regulatory requirements. Experience with validation in pharma, biotech, or medical devices. Familiarity with systems such as Sartorius and SAP More ❯

Computer System Validation (CSV) Engineer 📍 Location: Surrey | 💼 Contract | 🏭 Pharmaceutical Manufacturing We are on the hunt for Computer System Validation (CSV) Engineer to join our client for an exciting capital project involving a new production line. This role is critical in ensuring that all computerised systems are validated, compliant, and operate reliably in accordance with GxP and industry regulations. You will … What You Need: Degree in Science, Engineering, IT or related discipline, or equivalent practical experience. Strong knowledge of cGMP, GAMP 5 and relevant regulatory requirements. Experience with validation in pharma, biotech, or medical devices. Familiarity with systems such as Sartorius and SAP More ❯

Fimador are currently looking for a Product Owner to lead the delivery of innovative digital solutions that accelerate R&D across the pharmaceutical and life sciences sector. You’ll sit at the intersection of science, technology, and product strategy, translating complex laboratory workflows into powerful, intuitive software that enables better data, collaboration, and insight. What You’ll Do: Own and … voice of the scientist throughout the product lifecycle. About You: Experienced Product Owner or Technical Product Manager with a track record of delivering successful software products. Background working with pharma, biotech, or life sciences organisations — ideally within R&D or informatics. Comfortable engaging with scientists and lab-based users, understanding how they think and work. Strong grasp of scientific data More ❯

Fimador are currently looking for a Product Owner to lead the delivery of innovative digital solutions that accelerate R&D across the pharmaceutical and life sciences sector. You’ll sit at the intersection of science, technology, and product strategy, translating complex laboratory workflows into powerful, intuitive software that enables better data, collaboration, and insight. What You’ll Do: Own and … voice of the scientist throughout the product lifecycle. About You: Experienced Product Owner or Technical Product Manager with a track record of delivering successful software products. Background working with pharma, biotech, or life sciences organisations — ideally within R&D or informatics. Comfortable engaging with scientists and lab-based users, understanding how they think and work. Strong grasp of scientific data More ❯

ve grown to 30+ people, backed by significant investment, and led by a founding team with 60+ years of combined experience. We connect world-class talent with pioneering biotech, pharma, and AI-driven healthcare companies. About the Computational Sciences Division This is one of HLX’s fastest growing and highest billing teams, focusing on AI and Machine Learning in drug … Excited by new ideas, new clients, new opportunities The Role As a consultant, you will: Drive business development and attend client meetings across the US Partner with biotech and pharma companies to meet hiring needs Place candidates into top ML/AI drug discovery teams Build and grow client relationships Identify and engage top talent in computational biology, AI/ More ❯

ve grown to 30+ people, backed by significant investment, and led by a founding team with 60+ years of combined experience. We connect world-class talent with pioneering biotech, pharma, and AI-driven healthcare companies. About the Computational Sciences Division This is one of HLX’s fastest growing and highest billing teams, focusing on AI and Machine Learning in drug … Excited by new ideas, new clients, new opportunities The Role As a consultant, you will: Drive business development and attend client meetings across the US Partner with biotech and pharma companies to meet hiring needs Place candidates into top ML/AI drug discovery teams Build and grow client relationships Identify and engage top talent in computational biology, AI/ More ❯