1 to 25 of 50 Permanent Pharmaceutical Jobs in Reading

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 ❯

outcomes.While a data architect may be deployed across variety of different product teams areas, this role will initially focus on our Supply Product Group emphasizing data solutions to enable pharmaceutical drug manufacturing and quality. This role will be critical to unlocking the potential of Elanco’s supply chain data. A background in designing and delivering data capabilities to support manufacturing More ❯

Your new company Is a UK-based pharmaceutical company specialising in the neurology market. They focus on developing innovative products for chronic and serious medical conditions, with a particular emphasis on the treatment of Parkinson's disease. Your new role In this position, you will bridge the gap between IT and business operations, requiring a unique blend of technical expertise More ❯

satisfaction measured through structured feedback and surveys conducted periodically. Insights generated from metrics leading to Process and Quality Risks improvements. Qualifications Minimum of 6 years of experience in the pharmaceutical or CRO industry Minimum of 2 years of experience in Risk Based Quality Management Robust understanding of the drug development process and clinical trial execution Knowledge of industry regulatory standards … Learn more at https://jobs.iqvia.com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Other, Information Technology, and Management Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Director of Surveillance jobs in Reading, England, United Kingdom . We’re unlocking community knowledge More ❯

long-term DH portfolio requirements • Act as Business and/or Technical Owner for DH developed tools/systems Education & Experience At least 6 years of experience within a pharmaceutical company or a CRO is required. Strong understanding of Digital Health capabilities and their application in clinical trials. Excellent collaboration and communication skills, with the ability to work effectively with More ❯

long-term DH portfolio requirements Act as Business and/or Technical Owner for DH developed tools/systems Education & Experience At least 6 years of experience within a pharmaceutical company or a CRO is required. Strong understanding of Digital Health capabilities and their application in clinical trials. Excellent collaboration and communication skills, with the ability to work effectively with More ❯

Social network you want to login/join with: AG Consultancy & Apps Ltd are an SAP Gold Partner, SAP VAR Partner, SAP Quality Awards Gold Winner (Innovation) and UI Path Gold Partner with particular expertise within the SAP space. Working More ❯

Social network you want to login/join with: AG Consultancy & Apps Ltd are an SAP Gold Partner, SAP VAR Partner, SAP Quality Awards Gold Winner (Innovation) and UI Path Gold Partner with particular expertise within the SAP space. Working More ❯

technology, analytics, and human ingenuity to drive healthcare forward. Sales Executive – Life Sciences – Regulatory and Safety Technology Solutions Europe Based Our Regulatory Affairs and Drug Discovery Solutions team helps Pharma, Biopharma and MedTech companies handle regulatory and safety workflows more flexibly, productively, and efficiently. The Sales executive will be expected to lead key global or multi-country strategic and/… or in coordination with Global and Regional Sales Teams Requirements Must demonstrate a sustained successful track record selling enterprise solutions (i.e. products, consulting services, hosting and managed services) to Pharmaceutical, Biotech, Medical Device, and/or Clinical Research Organizations Demonstrated track record of success working with senior level management in a fast-paced growth environment is essential Full sales cycle More ❯

Oversee supplier systems, managing issues, risks, and escalations as needed. Ensure compliance with internal processes and external regulatory requirements. Required Qualifications: Previous experience working in the CRO, Healthcare or Pharmaceutical Industry Experience in Computer System Validation (CSV) and audit/inspection participation. Familiarity with Software Development Life Cycle (SDLC) and GAMP5 methodology. Strong understanding of Clinical Trial SaaS platforms/… health worldwide. Learn more at https://jobs.iqvia.com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Management and Manufacturing Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Sign in to set job alerts for “Digital Analyst” roles. Oxford, England, United Kingdom 3 weeks ago Staines-Upon More ❯

Join to apply for the Planning & Space Reporting Analyst role at Primark Join to apply for the Planning & Space Reporting Analyst role at Primark Get AI-powered advice on this job and more exclusive features. Planning and Space Reporting Analyst More ❯

in areas like Consulting, Analytics, RWE, and Advanced Analytics. Our Ideal Candidate The successful candidate will have a proven track record in most of the following areas: Expertise in Pharma & Life Sciences Commercial domain, understanding business strategies of large pharmaceutical companies gained in a professional service environment. Strong relationship-building and influencing skills. Excellent consultative selling skills and ability to More ❯

tables, figures, listings, define.xml). Experience And Qualifications Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry Strong programming skills in R/R Shiny Strong understanding of end to end Clinical Trials in Statistical Programming is a mandatory for this role. Exposure to Late Phase … Learn more at https://jobs.iqvia.com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Sign in to set job alerts for “Senior Clinical Scientist” roles. We’re unlocking community knowledge in a new More ❯

tables, figures, listings, define.xml). Experience And Qualifications Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry. Strong programming skills in R/R Shiny Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis … and population health worldwide. Learn more at https://jobs.iqvia.com Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Other Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Programming jobs in Reading, England, United Kingdom . Staines-Upon-Thames, England, United Kingdom More ❯

validated state of computerised systems Provide advice and act as project liaison Skills Degree in natural science or equivalent business experience Several years of Information Technology (IT) industry/pharmaceutical industry/medical devices industry/Regulatory Authority or otherwise relevant experience, preferably including Quality Assurance for Manufacturing, Pharmacovigilance and Clinical Development and Computerised System Validation and Data Integrity #J More ❯

Oversee supplier systems, managing issues, risks, and escalations as needed. Ensure compliance with internal processes and external regulatory requirements. Required Qualifications: Previous experience working in the CRO, Healthcare or Pharmaceutical Industry Experience in Computer System Validation (CSV) and audit/inspection participation . Familiarity with Software Development Life Cycle (SDLC) and GAMP5 methodology . Strong understanding of Clinical Trial SaaS More ❯

commercial awareness Knowledge of analytics platforms and enterprise BPS tooling (desirable) Degree qualified (preferred) Sector Focus CMI: Media, Telecom, and Information Services CBG/Life Sciences: Retail, CPG, and Pharma Why Apply? Join a top-tier BPS provider with major UK client partnerships Take ownership of a strategic role driving growth across major industries Access to global delivery capabilities and More ❯

travel and occasional global travel. Fluent written and spoken English skills and local language as needed. Experience (5+ yrs) in Sustainability/Corporate Responsibility. Experience within medical devices or pharma industry is preferable, but food and drink/electronics or other sectors impacted by EPR also considered. Have experience working at a management level. Must be able to lead and More ❯

development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients. We employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical … and legible at all times. Comply with all relevant SOPs and keep training file up to date. Qualifications and experience 2 years + cleaning experience. Relevant experience within a pharmaceutical environment. Excellent communication skills, written and verbal. Application Requirements When applying for a position with Quotient Sciences, you must be aged 18 years or over and not have been debarred More ❯

up to date on the latest industry tech and developments What we’re looking for: Solid automation engineering experience—ideally 3+ years Strong background in the life sciences or pharma sectors Confident with PLC programming and automation systems Great communication skills and a customer-focused mindset Based in the UK with the right to work—unfortunately, we can’t sponsor More ❯

Python , familiar with software development best practices . Practical experience with TensorFlow and/or PyTorch . Preferred Qualifications 3+ years post-graduate experience in academia or biotech/pharma, applying ML/AI to biological datasets . Prior exposure to immunology , especially TCR/BCR repertoire analysis, or experience with protein design & or biologics. Deep expertise in at least More ❯

Value and Access Strategy, Pathway Analytics, Transformation, Case Finding, Training and Development Market Engagement and Activation, Patient Engagement and Clinical Support Nursing Services Clinical Pharmacists Training Services Our Clients: Pharmaceutical, Med Tech, Biopharma, Startups, NHS, Consumer Health, Biotech, Med Devices, Healthcare Providers What You Need: Minimum of 2 years in a related field, or an equivalent combination of education, training More ❯

Social network you want to login/join with: Type: Full time, hybrid (2 days in the office). IQVIA are looking for an Ecommerce Manager to join our client’s team! If you are passionate, driven, and thrive in More ❯

1 week ago Be among the first 25 applicants Direct message the job poster from Simpro Software First Things First - What We Can Offer You A generous annual leave entitlement plus a personal leave entitlement Private Health Insurance Employee Assistance More ❯

4 days ago Be among the first 25 applicants Job Description Please note this role requires travel, and therefore a fully expensed van is included. covering High Wycombe, Maidenhead, Slough, Bracknell, Reading & Wokingham. As the UK’s largest fibre-only More ❯