1 to 25 of 890 Remote Pharmaceutical Jobs

Key Words Software, SDLC, Process, Agile Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Management and Manufacturing Industries Biotechnology Research, Pharmaceutical Manufacturing, and Appliances, Electrical, and Electronics Manufacturing Referrals increase your chances of interviewing at Waters Corporation by 2x Get notified about new Senior Business Process Analyst jobs in Wilmslow, England 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 ❯

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 ❯

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 ❯

clients harness the full potential of the most innovative solutions on the market. About the role We are seeking a highly skilled IT Senior Consultant with expertise in the pharmaceutical industry to join our System Operations team. The successful candidate will be responsible for providing post-implementation consultancy, designing, implementing and supporting technology solutions, L3 support, and ensuring optimal performance … of critical IT systems such as Veeva Vault, Veeva CRM, and Salesforce. This role requires a deep understanding of pharmaceutical processes, regulatory requirements, and advanced IT knowledge to support our business objectives and optimize our IT infrastructure. As a Senior Consultant your responsibilities include: Lead configuration initiatives to optimize IT solutions, ensuring they meet evolving business and regulatory needs. Provide … with a preponderance of clients to be served in Germany. What makes you the best person for this job? The ideal candidate for the L3 CRM Consultant position in Pharma is an experienced IT professional with a robust background in managing CRM or Data management systems. They are adept at troubleshooting complex issues, providing expert post-implementation support, and optimizing More ❯

click here: https://careers.jazzpharma.com/benefits.html. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Education and Training Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Jazz Pharmaceuticals by 2x Get notified about new Principal jobs in London, England, United Kingdom . London, England, United Kingdom 6 days More ❯

with a state-of-the-art GenAI application with multi-agent workflow that helps with the drug discovery portfolio management. It’s an opportunity to revolutionize ML in the pharmaceutical industry and collaborate with a diverse, strong and upbeat cross-functional team. Your key responsibilities will include: Collaborative Innovation: working directly with AI/ML scientists on optimization and production … target discovery unit with a focus on identifying novel, game-changing therapies for patients. The site is a fusion of the best of academia, biotech, software engineering, and big pharma to realize cutting-edge biology. NNRCO operates at the boundaries of frontier science with a mandate to find dynamic, agile, and distinctive new ways of working to diversify the company 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 ❯

At Reach Industries, we believe that scientists are solving some of the world's most pressing challenges, from combating climate change to developing vaccines and new treatments for diseases yet their tools are still poor. Our AI powered software platform More ❯

expected to embody its contents each day. What You Will Do You will work closely with our scientific end-users to design, architect, and deliver highly impactful solutions to pharmaceutical and biotech customers. You will work to understand scientists' and R&D IT analysts' needs, analyze their data environment, assist in the design and implementation of our solutions, and aid … to technical solutions ROI Calculation: Determine potential return on investment for proposed solutions Industry Knowledge: Understand industry-specific challenges and trends to tailor solutions accordingly in the Biopharma and Pharma vertical Soft Skills: Communication: Translate complex technical topics into easily digestible content for non-technical stakeholders Presentation Skills: Deliver compelling presentations to both small and large audiences Relationship Building: Cultivate … LES, analytics, visualization suites Deep understanding of drug discovery, development, and manufacturing processes. Experience in large molecule or new modalities is a plus Proficient in enterprise sales within the pharmaceutical sector Skilled Intellectually curious: Unwavering drive to learn and know more every day Ability to deal with ambiguity and thrive in a constantly changing and evolving work environment Experience with More ❯

a degree. Five years or more of relevant experience in supporting the operational feasibility, design, and analytics of clinical trial operations. Experience working at a Clinical Research Organization or Pharmaceutical company conducting study feasibility, site selection analytics and study performance analytics. A thorough understanding of clinical trial design, execution, and regulatory requirements. Expert skills in Excel and PowerPoint. Proficiency in 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 ❯

engage and communicate effectively with executive-level stakeholders in a client-facing role. Strong collaborative communication and influencing skills, ensuring alignment across diverse teams. Deep experience in life sciences, pharmaceutical workflows, or scientific research environments—especially related to drug discovery, biologics, automation, or emerging modalities. Background in GxP compliance or familiarity with Good Laboratory Practices (GLP). Bachelor’s degree 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 ❯

systems, control systems and building management systems Experience with IT/OT implementation with DCS, MES, BMS, PLC, OPC, HPLC, GC, LIMs, lab analyzers Prior experience working for a Pharmaceutical company required Experience working with virtual environment (VMware/Hyper-V) and/or cloud platform (AWS preferred) Experience working with RDBMS (SQL Server or Oracle) Experience working with application More ❯

At Reach Industries, we believe that scientists are solving some of the world's most pressing challenges, from combating climate change to developing vaccines and new treatments for diseases yet their tools are still poor. Our AI powered software platform More ❯

our goals: Required Qualifications, Knowledge, Skills and Experience Bachelor’s degree in communication related field or in Computer Science discipline together with significant demonstrable engagement experience within IT or Pharma company. Strong and dynamic communicator with excellent verbal and written communications skills Ability to manage time effectively without supervision and to organize, prioritize and deliver tasks and projects with a … CMS) website at https://openpaymentsdata.cms.gov/Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Engineering and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at GSK by 2x Get notified about new Engineering Team Lead jobs in London, England, United Kingdom . London, England, United Kingdom 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 ❯

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 ❯

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 ❯

making. Experience in mentoring and guiding junior team members. Strong customer focus and understanding of customer needs and market trends. Familiarity with Agile development methodologies. Experience on working with pharmaceutical and chemical companies as well as academia Master degree in chemistry or related sciences Good to have: Product management certification (Agile, Scrum, SVPG) Experience in working in pharmaceutical companies in 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 ❯