1 to 25 of 837 Pharmaceutical Jobs

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 ❯

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 ❯

of experience in managing MES projects with a minimum of 3 years dedicated to PAS-X implementations. Proven track record of successful PAS-X rollouts in GMP manufacturing environments (pharma/biotech). In-depth knowledge of PAS-X architecture, MBR design principles, and standard modules (eBR, Equipment Management, Weigh & Dispense, etc.). Strong grasp of GxP, CSV, GAMP5, and …/88 compliance. Excellent leadership, stakeholder management, and communication skills. What's in it for you? Opportunity to lead high-impact PAS-X projects in a globally recognized pharmaceutical environment. Competitive compensation and benefits. Work with advanced MES technology and shape the future of digital manufacturing. Collaborative and high-performance culture with room for career growth. 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 ❯

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 ❯

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 … Medicare and Medicaid Services (CMS) website at Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at GSK by 2x Sign in to set job alerts for “Director of Analytics” roles. London, England, United Kingdom 5 days ago Associate 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 ❯

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 ❯

related to Life Sciences, Computer Science, Automation, Bioengineering or related study. You have strong experience in cleaning, process equipements. You have at least 5 years of experience in a pharmaceutical with a focus on delivering solution. You have excellent understanding of GxP regulations, 21 CFR Part 11, Eudralex Annex 11 or other international requirements. You are proficiency in French and More ❯

technology streams (data, AI, computer 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 have solid PMO experience in More ❯

technology streams (data, AI, computer 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 have solid PMO experience in More ❯

technology streams (data, AI, computer 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 is a must Strong understanding of EU work culture and fluency in relevant languages In-depth knowledge of EU architectural mandates, best practices and More ❯

technology streams (data, AI, computer 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 is a must Strong understanding of EU work culture and fluency in relevant languages In-depth knowledge of EU architectural mandates, best practices and More ❯

Associate Director of Laboratory Engineering and Technology - Site Lead Oxford Join to apply for the Associate Director of Laboratory Engineering and Technology - Site Lead Oxford role at Vertex Pharmaceuticals Continue with Google Continue with Google Associate Director of Laboratory Engineering More ❯

proud to be partnering with a well-established CRO and analytical testing organisation operating at the forefront of inhalation and drug delivery science. With a strong presence in the pharmaceutical development landscape, this company is recognised for its specialist expertise in the testing and development of inhaled and nasal drug products, providing essential support to global pharmaceutical and biotech clients. … This organisation is based in the United Kingdom and focuses on the development and testing of inhalable and nasal pharmaceutical products. They work closely with pharmaceutical companies to ensure product safety, efficacy, and regulatory compliance. PRIMARY PURPOSE SUMMARY This position is responsible for leading and managing a small team of Computational Scientists. The team supports pharmaceutical development programs, clients, and 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 ❯