201 to 225 of 361 Pharmaceutical Jobs in the UK

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 ❯

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 ❯

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 ❯

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 ❯

Here at Optum we have an opportunity for a tech-focused Delivery Lead to join us on a fixed term contract until the end of 2026. We are a tech for good business, and everyone who works here genuinely makes 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 ❯

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 ❯

Robert Half have partnered with one of our Pharmaceutical manufacturing organisations to help them recruit for an experience Snowflake Data Engineer on an initial 6 months experienced based out of their London office. You will play a key role in designing and managing our Snowflake data warehouse and leveraging dbt (Data Build Tool) to transform raw data into reliable, analysis … business needs. Requirements: Bachelor's degree in Computer Science, Data Engineering, Information Systems, or related field. 3-5+ years of experience as a Data Engineer, ideally in a pharmaceutical, biotech, or regulated manufacturing environment. Strong hands-on experience with: Snowflake (architecture, performance tuning, cost optimisation) DBT (model development, testing, documentation, deployment) SQL (advanced query optimisation and debugging) Experience with 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 ❯

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 ❯

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 ❯

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 ❯

global institutions. Our comprehensive in-house capabilities assist partners in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National … join the Company and support our expanding business and scientific efforts. The selected candidates will be responsible for developing and fostering relationships with key decision-makers at Biotech and Pharmaceutical companies and Not-For-Profit Organizations to secure business opportunities for the Company. The successful candidates will be self-motivated, success-driven individuals who are well networked within the life … related field required Working knowledge of drug discovery Fluent in English (both written and oral) 5+ years of business development/sales experience in life sciences/biotech/pharma Proven sales track record in life sciences industry - a preference will be given to a track record of sales in the drug discovery arena. A strong network of senior level More ❯