1 to 25 of 766 Permanent 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 ❯

diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. COVID-19 Statement All U.S. colleagues are required to disclose 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 ❯

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 ❯

Site Name: UK - Hertfordshire - Stevenage, Cambridge MA, UK - London, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: Jul The pharmaceutical industry is undergoing rapid digital transformation, and our R&D Development organization is investing heavily in digital health technologies to revolutionize drug development. This new role, Senior Director, Digital Health Innovation and Implementation , will be crucial in driving the … on performance and ROI of digital health initiatives within Clinical Operations and across Development. Compliance & Regulatory : Stay informed about relevant regulations and guidelines related to digital health in the pharmaceutical industry. Ensure all implemented solutions adhere to regulatory requirements. Qualifications and Experience: Required Qualifications: Bachelor's degree in a relevant field (computer science, information technology, life sciences, or related field … skill and experience managing multiple complex projects simultaneously, including budget management and resource allocation. Strong understanding of regulatory requirements and industry standards related to digital health solutions in the pharmaceutical industry. Experience working within a regulated environment is essential. Preferred Qualifications: Advanced degree (MS, PhD, or MBA) is preferred. Strategic thinker with a strong grasp of operational realities in clinical 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 ❯

to lift, move or carry equipment up to 10lb frequently, and up to 25lbs infrequently. It would be a plus if you also possess previous experience in: Life Science, Pharmaceutical, Medical Device or Biopharma manufacturing environments. Analytical and problem-solving skills. Strong communication skills (written and oral) with associates at all levels of the organization. Cytiva, a Danaher operating company More ❯

evolution/strategic directions, and new trends/issues. Establish a strong site culture based in Lilly values, expectations, and operational excellence standards. What You Should Bring (preferred skills: Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP) Effective people and team leadership skills Ability to manage and contribute to multiple concurrent activities and adapt to changes in priorities. Ability to … Requirements: Bachelor's degree in engineering, Computer Science, Information Technology, or a related technical field. Minimum 2 years of experience working with Manufacturing Execution Systems (MES), with in the pharmaceutical or life sciences industry. 2+ years technical ability to develop and integrate MES solutions. Experience with MES platforms such as PMX, PharmaSuite (Rockwell), Syncade-DeltaV MES (Emerson), Werum PAS-X More ❯

responsible for designing new operating models for Operations analytics (network and supplychain, manufacturing, distribution, quality etc). Essential Skills Strong business analysis experience and knowledge of ERP analytics in pharma operations. Experience of design, build and testing of the analytics solution in SAP Team leadership management (task management)/experience Experience in working with large and sophisticated data sets in … to dispatch door; integrated clinical supply management; Leading multiple teams across geographies. Regulatory experience, e.g. GxP, SOx. Familiarity with data science concepts and use cases in Operations. Bio-Tech, Pharmaceutical or Life Sciences experience. UX experience. Certifications such as SAP, Project Management, Business Intelligence, Data Management, Lean Framework. Experience in large scale, complex & multi-year projects. Workshop Management. This contract 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 ❯

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 ❯

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 ❯

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 ❯

evolution/strategic directions, and new trends/issues. Establish a strong site culture based in Lilly values, expectations, and operational excellence standards. What You Should Bring (preferred skills: Pharmaceutical Manufacturing Regulatory compliance knowledge and experience (cGMP) Effective people and team leadership skills Ability to manage and contribute to multiple concurrent activities and adapt to changes in priorities. Ability to … Requirements: Bachelor's degree in engineering, Computer Science, Information Technology, or a related technical field. Minimum 2 years of experience working with Manufacturing Execution Systems (MES), with in the pharmaceutical or life sciences industry. 2+ years technical ability to develop and integrate MES solutions. Experience with MES platforms such as PMX, PharmaSuite (Rockwell), Syncade-DeltaV MES (Emerson), Werum PAS-X More ❯