1 to 25 of 269 Remote Pharmaceutical Jobs

and internal policies. Collaborate with legal and compliance teams to evaluate subcontracting needs. Candidate requirements: More than 10 years experience within the field of Pharma, Biotech or CRO More than 5 years experience in an external or client facing project management role Will have a good working knowledge of global … pharmaceutical and supply chain regulations including but not limited to cGDP, cGMP Experienced line manager capable of leading and developing teams across geographies Experienced in system integration and data management to allow business reporting and oversight Experienced in client or external interactions and confident in leading conversations at all levels … workforce of more than 3,000 spread across Ireland, United Kingdom, Mainland Europe, MENA and the USA, Uniphar is a trusted global partner to pharma and medtech manufacturers, working to improve patient access to medicines and treatments around the world. Uniphar provides outsourced and specialised services to its clients, leveraging More ❯

software development of key manufacturing systems such as Supervisory Control or Data Acquisition (SCADA), Systech, FactoryTalk Asset Centre applications that support manufacturing, preferably biotechnology, pharmaceutical, or related industry 5+ years experience crafting, developing, deploying, and operating automated solutions across SaaS, Cloud, On-prem and custom software developed platforms Experience with More ❯

of key manufacturing systems such as Rockwell FactoryTalk, PAS-X MES, AVEVA PI, Siemens Desigo and SAP EWM applications that support manufacturing, preferably biotechnology, pharmaceutical, or related industry. Hands-on experience with computerized systems including troubleshooting, reliability, and performance improvements. Expertise with translating business requirements/user stories to technical More ❯

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 More ❯

of key manufacturing systems such as Rockwell FactoryTalk, PAS-X MES, AVEVA PI, Siemens Desigo and SAP EWM applications that support manufacturing, preferably biotechnology, pharmaceutical, or related industry. Hands-on experience with computerized systems including troubleshooting, reliability, and performance improvements. Expertise with translating business requirements/user stories to technical More ❯

developing with various Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure, integration, and data management. Experience in industries such as pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Knowledge of healthcare industry regulations, data security, compliance standards (e.g., GDPR), and EDI standards (e.g., FHIR More ❯

features/functions. Basic Qualifications BS, MS, or PhD in a field of science, engineering, pharmacy, or medicine 5+ years of experience in the pharmaceutical industry, in areas of cGMPs/cGxP's Demonstrated experience with understanding and use of quality systems and the external regulatory environment Demonstrated experience in More ❯

various relevant Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure tools, integration, and data. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. More ❯

leads and inspires colleagues. Strong influencing and leadership skills. Understands influencing, stakeholder management and negotiation strategies. The Client is ideally seeking someone from a Pharmaceutical or Bio Science background and who understands how to work with the government and government funding. This position will manage 15 people within the IT More ❯

study. You have strong experience in Analytical, Automated and/or Computer Systems validation. You have at least 5 years of experience in a pharmaceutical or regulated QC environment with a focus on delivering solution. You have excellent understanding of GxP regulations, 21 CFR Part 11, Eudralex Annex 11 or More ❯

as assigned. EXPERIENCE Required Skills: Minimum of 10 years experience in automation or equivalent type of process controls Minimum 10 years experience in Bio-Pharmaceutical or equivalent type of life science industry Minimum of 5 years experience with Korber PAS-X MES Suite Experience with system implementation and SDLC requirements More ❯

Industries : You will not focus on a specific sector, you may work for clients active in the following sectors: Transport, logistics, manufacturing, oil & gas, pharma, retail, service providers, etc. Shape the future with confidence. The Opportunity: Your Next Adventure Awaits? Technology Risk addresses the latter three within EY Consulting, allowing More ❯

Full Time Who is Instem? I nstem is a global leader in SaaS solutions for the life sciences industry, providing cutting-edge technology to pharmaceutical companies, contract research organizations (CROs), and academic institutions. Our solutions accelerate drug discovery, study management, and regulatory submission, helping researchers make better, faster decisions. Why More ❯

Knowledge of tools like LevelPath, MuleSoft, and EDF for integrations. Experience delivering in SAFe or Agile environments. Experience working in regulated global environments (e.g., pharma, manufacturing, life sciences) is a strong plus. Professional Certifications (Preferred): SAFe Product Owner/Manager certification. SAP certification in MM or Ariba is a plus. More ❯

experience in a GMP environment Preferred Qualifications: Advance degree in Computer, Electrical, Mechanical, Chemical Engineering, or Biomedical Engineering Knowledge and/or experience of pharmaceutical/biotech processes, especially in the area of final drug product operations Knowledge in Data Integrity and Security Extensive understanding and background in programming, design More ❯

innovations, positioning them within broader industry trends to inform internal teams and external stakeholders. Lead simultaneous client facing projects across ZS Discovery to reinvent pharmaceutical discovery, elucidate complex disease biology and pioneer novel therapeutics. Provide expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics More ❯

headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit . As a Senior Data Analytics Engineer in Operational Intelligence, you will work collaboratively with stakeholders More ❯

Experience managing data architecture, engineering, and reporting across Commercial, Medical Affairs, and Finance. Strong knowledge of enterprise and external Commercial data sources in the Pharma/BioPharma industry. Education/Qualifications: Bachelor's degree in Computer Science, Information Systems, a STEM field or equivalent. Preferably with a Master's degree More ❯

Working time: Full-time Mobile Working: mobile working possible A. Menarini Research & Business Service GmbH, Menarini GmbH for short, is an affiliate of the pharmaceutical company BERLIN-CHEMIE. Both companies belong to Italy's Menarini Group. We operate in an international setting with 17,000 employees at the group and More ❯

looking for BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Proficient in MS Office (Word, Excel and More ❯

/regulated industry • 3 to 5 years' experience in Analytical Instruments validation • 3 to 5 years working in the Quality area in biotech or pharma • Experience in Deviations, CAPAs and Change Control Management • Strong background and implementation experience on industry regulations (e.g., FDA CSV, FDA CSA, 21CFR210, 211, 820, Part More ❯

research. Skills and Competencies: Proven track record of developing and executing innovative marketing campaigns within the Enterprise sector, with particular experience in life sciences (pharmaceutical, medical devices, biotech), tech, and manufacturing. Creative marketing abilities with excellent persuasive writing skills. Strong understanding of various research roles and responsibilities in the Enterprise More ❯

GED and 10 years of Manufacturing Process automation/Information system experience Preferred Qualifications: Demonstrable experience in a manufacturing environment with ability in the Pharmaceutical or Biotechnology industries. Direct knowledge of Automation design, experience in process control engineering and troubleshooting with GMP biopharmaceutical production facility equipment/systems such as More ❯

working with virtual/Agile teams in different locations, aligning and adapting different work, culture, and communication styles. Experience with designing and development of pharmaceutical life science products Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We More ❯

patient trials with a success rate of up to 91.3%. Mediktor's clients include health plans, hospitals and health systems, telemedicine companies and pharmaceutical companies. Visit to find out more. You can try out our showcase application for yourself. We would love to hear your feedback: Mediktor in the More ❯