1 to 25 of 201 Remote Pharmaceutical Jobs

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 ❯

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 ❯

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 ❯

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 ❯

o Collaborate with the technical an cross functional team to ensure seamless delivery of the solution Essential Qualifications: o Strong business analysis experience and knowledge of ERP analytics in pharma operations. Experience of design, build and testing of the analytics solution in SAP o Team leadership management (task management)/experience o Experience in working with large and sophisticated data … clinical supply management; o Leading multiple teams across geographies. o Regulatory experience, eg GxP, SOx. o Familiarity with data science concepts and use cases in Operations. o Bio-Tech, Pharmaceutical or Life Sciences experience. o UX experience. o Certifications such as SAP, Project Management, Business Intelligence, Data Management, Lean Framework. o Experience in large scale, complex & multi-year projects. o 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 ❯

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 ❯

in technical support/field service highly valuable - this demonstrates your ability to internalize complexities and tailor explanations for a given audience Familiarity with enterprise sales processs within the pharmaceutical sector Experience with AWS application stack Competitive Salary and equity in a fast-growing company. Supportive, team-oriented culture of continuous improvement. Generous paid time off (PTO). Flexible working 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 ❯

s degree in Automation Engineering, Mechatronics, Electrical Engineering, Computer Science, or related field. Experience in designing and implementing automation solutions, ideally in R&D or manufacturing environments (food or pharma experience is a plus). Proven experience in writing User Requirements Specifications (URS) and effectively collaborating with external vendors, integrators, or partners throughout the project lifecycle. Proficiency in robotic systems 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 ❯

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 ❯

Our top Nuclear client is looking for a Senior Database Engineer to join their team in Warrington or Stockton Our Client has a requirement for a Database Engineer, who will be required to work on a contract basis in Warrington More ❯

Our top Nuclear client is looking for a Senior Database Engineer to join their team in Warrington or Stockton Our Client has a requirement for a Database Engineer, who will be required to work on a contract basis in Warrington More ❯

take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology, and consulting to cater to the unique needs of small, medium, and large pharmaceutical companies. Job Title: Consulting Technology Programme Manager (PV Systems) Job Type : Full-Time Job Description: Programme Manager will be responsible for the successful orchestration of interrelated projects that together deliver … to deliver program outcomes on time, within budget, and to high quality standards. They must be highly experienced, strategic thinker with deep domain expertise in software delivery for the pharmaceutical industry—particularly in the areas of pharmacovigilance, safety, and regulatory technology. Key Responsibilities: Define, lead, and manage the successful execution of complex, multi-workstream programmes for pharmaceutical clients. Align programme … Master's degree in Computer Science, Information Technology, Project Management, or a related field. 12+ years of experience in client facing project and programme management delivering software solutions to pharmaceutical or life sciences clients. Excellent leadership, strategic thinking, and stakeholder management skills. Proven ability to manage crossfunctional, geographically distributed teams and external vendors in a matrixed environment. Knowledge of regulatory 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 ❯

to £40k (depending on experience) Sonrai is a Belfast-based AI data discovery company on a mission to help save patient lives through AI technology. We enable Biotech and Pharma companies to reduce the cost, time, and risk from early discovery to clinical trials, accelerate drug, biomarker, and diagnostics, maintain a secure and compliant Trusted Research Environment, and effectively and … our strategy. It's a great time to be joining Sonrai; over the past two years, we have: Successfully grown our customer base across a range of biotech and pharma organisations globally Grown our team to 35+ and won multiple awards Opportunity & Responsibilities The Customer Success Manager will work closely with the Director of Customer Success and the wider Sonrai More ❯

global experience. We are in search of a Technical Event Project Manager to join our team to ensure the successful project management and delivery of exhibition booths for our Pharmaceutical Clients. About the Technical Event Project Manager As the Technical Event Project Manager, you will have experience in the design and project management of exhibition booths with a keen eye … Event Project Manager for your technical expertise in the end-to-end production of exhibition booths in the life sciences industry. You will have worked with a variety of Pharmaceutical Clients and will have utilized your creative and technical skills to support the design and build of exhibition booths in congress halls across Europe. You will be proficient at working More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯

strong technical documentation writing skills Strong interpersonal, written, and verbal communication skills Desirable experience: Experience in the EC&I industry or highly regulated industries such as Nuclear, MOD, or Pharmaceutical Experience with cloud-based platforms like GCP, AWS, or Azure Knowledge of database clustering, load-balancing, and redundancy Familiarity with integrated SCADA control system applications Experience in OT Cyber Security More ❯