1 to 25 of 274 Remote Pharmaceutical Jobs

If you are a current Jazz employee please apply via the Internal Career site. Do you have the right skills and experience for this role Read on to find out, and make your application. Jazz Pharmaceuticals is a global biopharma More ❯

If you are a current Jazz employee please apply via the Internal Career site. Do you have the right skills and experience for this role Read on to find out, and make your application. Jazz Pharmaceuticals is a global biopharma 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 ❯

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 ❯

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 ❯

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 ❯

and One STADA to achieve ambitious goals and shape the successful future of STADA. Britannia Pharmaceuticals , part of the STADA Arzneimittel AG group of companies, is a UK based pharmaceutical company specialising in the neurology market. Britannia focuses on innovative products for chronic and serious medical conditions, and in particular, the treatment of Parkinson's disease. We are highly committed More ❯

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 cover modern service assignments, for example in the area of research and development, IT, engineering, HR, purchasing, logistics or More ❯

BS, BA) or equivalent professional experience is required, preferably in Health Sciences or Data Sciences. Advanced degrees preferred (e.g., Masters, PhD). Minimum 8-12 years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry! Knowledge of trial site operations and study execution Strong knowledge of regulatory guidelines (e.g., ICH-GCP). Demonstrated strong understanding of More ❯

building a better working world. 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 you to act as a More ❯

insights based on ZS-driven 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, bulk or single cell RNA More ❯

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to advancements across our robust pipeline of innovative therapeutics in oncology and laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. The Senior Principal 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 … technical solutions to business leadership 18-24 month project duration with hybrid work model and up to 25% travel for stakeholder meetings and go-live support Preferred: SAP certifications, pharmaceutical supply chain/serialization knowledge, DevOps/CI-CD experience, Master Data Governance (MDG) expertise Location: Luton/Macclesfield 3 days onsite More ❯

In this role, you will define the product roadmap, align cross-functional teams, and ensure that our AI-driven solutions deliver measurable value to clinical operations teams across the pharma and biotech landscape. You will collaborate with cross-functional teams from tech and business to build agentic capabilities from concept to production. Key Responsibilities Product Strategy and Vision: Define and More ❯

skills. Experience within a GMP production environment. Fluency in written and spoken English; Dutch language skills are a plus. Skills: Critical evaluation and interpretation of data. Strong knowledge of pharmaceutical manufacturing processes and quality systems. Commitment to staying current with industry trends and regulatory updates. Social skills such as tact, listening, service attitude, and persuasiveness. Ability to create and review More ❯

enabled self-services. Your skills and experience Bachelor's degree with a preferred focus in Information Technology, Computer Science, or related field or equivalent combination of education and experience. Pharma/Biotech or similarly regulated environment experience preferred. IT Security Industry certifications (CISM, CISSP, CISA, etc.) desirable. Experience with Large-scale Active directory implementations, with expert knowledge (7+ years) in More ❯

Deep knowledge of Industry's QA and QC processes alongside all QM elements in one or more of the following sectors is an advantage: Aerospace and Defence, Consumer Products, Pharma or Discrete Manufacturing. Leadership experience across small to medium-sized teams, both onshore and offshore. Commitment, flexibility, thought leadership and a hunger to develop your career within the SAP SCM More ❯

world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services More ❯

a variety of sectors. Exposure to working in or with Software Development teams is beneficial. Familiarity with operations and security in industrial sectors such as, Energy, Manufacturing, Marine and Pharmaceutical industry sectors would be beneficial. Familiarity with predominant public cloud providers (Azure, AWS, GCP) Understanding of Industry trends in cloud technologies for public, private and hybrid cloud deployments Bachelor's More ❯

to the client's business Recruit and develop high-quality individuals to grow the Analytics consulting team Lead a data science team Requirements 12+ years of experience with the pharmaceutical industry Background in the pharmaceutical industry analytics programs - specific experience delivering programs related to Segmentation & Targeting, Commercial Analytics, Omni-channel, Marketing Mix Modelling, and Field Force sizing and optimization Strong … track record of experience owning client relationships and managing $2M+ in annual program delivery Strong understanding of how different pharmaceutical data sets are used to make key decisions and go-to-market strategies - specifically sales & claims data. Deep understanding of data availability by the EU market Core management consulting skills, including workshop facilitation, client presentations, project management, and ability to More ❯

Salesforce Administrator Locations UK Type home-based Position type Full-time, permanent role About Labcorp: We are a global leader in innovative and comprehensive laboratory services, helping doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. With over 60,000 employees, our cutting-edge diagnostics and drug development capabilities address major health challenges, accelerate healthcare breakthroughs, and … policies. Training & development: Access various training formats to grow your career and develop a global mindset. Why us: Labcorp is a leader in diagnostics and drug development, supporting global pharmaceutical advancements. Top provider in clinical trial data and early-phase solutions. First to receive FDA approval for at-home COVID-19 testing kits. Recognized as one of Forbes' World's More ❯

Strong knowledge of procurement models, inventory flows, and indirect/direct purchasing Hands-on configuration skills and a deep understanding of business processes Experience in global rollouts-especially in pharma, manufacturing, or retail is a plus Familiarity with SAP Ariba and integration scenarios (nice to have) Excellent communication skills and stakeholder confidence-you're comfortable leading from the from the More ❯

and ensure timely, high-quality deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis and machine learning. Experience working with high-dimensional biological datasets (e.g., transcriptomics More ❯

including Elastic, Kafka, Kubernetes and Luigi. Finally, you will have the exciting opportunity to look behind the scenes of our many industrial customers from various sectors, including (petro-) chemical, pharma and biotech, paper and pulp, automotive, metallurgy and food-and-beverage. Here's a selection of some projects where we've built software solutions for our customers: AI-based biometric More ❯

optimization, and experimental design. Preferred Qualifications & Skills: Please note the following skills are not necessary, just preferred, if you do not have them, please still apply: Prior experience in pharmaceutical R&D and drug discovery workflows. Familiarity with biomedical datasets such as omics, EHR, imaging, or clinical trial data. Familiarity with FAIR data principles, real-world evidence (RWE), or synthetic More ❯