1 to 25 of 186 Remote Permanent 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 ❯

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 ❯

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 ❯

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 ❯

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 ❯

Logistics/WM Consultant with this market leading consultancy who specialise within the UK government and defence sector and are looking to expand their footprint within the financial services, pharmaceutical, manufacturing and retail sectors. They are expanding their SAP practice across the UK and Europe and are looking for Senior SAP S/4HANA Logistic Consultant to join their growing 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 ❯

projects simultaneously Own responsibility for work product quality and relevance to client decisions Lead cross functional teams in the delivery of complex SCM consulting engagements/programs in the pharma/Life Sciences industry Update senior leaders and prepare and present the majority of client presentations Manage senior client relationships and serve as the primary point of contact for the 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 ❯

Spherical Search have partnered up with a well-known Analytical Services/CRO company who specialise in the inhalation and nasal drug delivery space , working with a range of pharmaceutical companies and drug delivery device developers. My client is currently looking for a Project Manager to work at their Cwmbran site. This would be a hybrid role with the option More ❯

Senior Data Analyst – RWE | Global CRO – Client FSP | UK & Europe | Home based | We’re hiring a Senior Data Analyst to join our clients expanding Real-World Evidence team where you will be fully embedded within our client’s FSP model More ❯

Who we are We are a London tech startup on the lookout for bright, motivated and self-driven individuals to join the team. Who you are You are a recent PhD graduate, or about to graduate, in a STEM field More ❯

in ensuring compliance with critical international standards and regulations across a rapidly expanding platform. As a Compliance Manager for the EMEA region, you'll lead efforts to support regulated pharma environments, manage internal and external audits, and influence the company's quality strategy in collaboration with technical and customer-facing teams. If you are experienced in GxP, ISO, and EU … sales cycles and customer engagements. Maintain comprehensive documentation and drive cross-functional consistency across regulatory processes. 10+ years of experience in software lifecycle management and validation, with emphasis on pharma or biotech compliance. Solid knowledge of EU regulatory frameworks (e.g., GxP, 21 CFR Part 11, Annex 11). Experience preparing for and navigating ISO, SOC, and other third-party compliance … s degree in computer science, life sciences, or a related field. Preferred: Advanced degree in compliance or regulatory affairs; ISO 9001 Lead Auditor certification; experience working with EU-based pharmaceutical companies. Competitive salary and equity in a high-growth organization. Remote-first culture with flexible working arrangements across EMEA. Generous paid time off (PTO) to support work-life balance. A More ❯

global institutions. Our comprehensive in-house capabilities assist partners in achieving key milestones and progressing towards clinical readiness, positioning IRBM as a major player in driving innovation in the pharmaceutical and biotech fields. IRBM Group also has a GMP - certified Contract Development and Manufacturing Organization (CDMO), ADVAXIA Biologics. ADVAXIA is authorized to produce investigational medicinal products by the Italian National … join the Company and support our expanding business and scientific efforts. The selected candidates will be responsible for developing and fostering relationships with key decision-makers at Biotech and Pharmaceutical companies and Not-For-Profit Organizations to secure business opportunities for the Company. The successful candidates will be self-motivated, success-driven individuals who are well networked within the life … related field required Working knowledge of drug discovery Fluent in English (both written and oral) 5+ years of business development/sales experience in life sciences/biotech/pharma Proven sales track record in life sciences industry - a preference will be given to a track record of sales in the drug discovery arena. A strong network of senior level More ❯

when you work at Charles River, you will be the difference every day for patients across the globe. Job Summary Do you have lab experience in the biotech or pharma industry? Are you ready for your next laboratory position? Our In Vitro Biology team in Portishead are recruiting, could you be the next team member in our lab? As an … Training is provided for all scientific tasks and processing. Advantageous but NOT essential: Educated to BSc level. MSc preferred within a relevant scientific discipline. Relevant CRO/Biotech/Pharma industry in specialism. General cell biology and in vivo processing support. What We Offer You A very comprehensive benefits package from day one, including a generous pension contribution, private medical … countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our More ❯