Saffron Walden, Essex, South East, United Kingdom Hybrid / WFH Options
EMBL-EBI
between the European Bioinformatics Institute (EMBL-EBI), a global leader in the management, integration and analysis of public domain life science data; world-leading pharmaceutical companies GSK, Sanofi, Bristol Myers Squibb, Pfizer and Genentech; and the Wellcome Sanger Institute. Generative AI has revolutionised the way we interact with knowledge. To more »
Saffron Walden, Essex, South East, United Kingdom Hybrid / WFH Options
EMBL-EBI
between the European Bioinformatics Institute (EMBL-EBI), a global leader in the management, integration and analysis of public domain life science data; world-leading pharmaceutical companies GSK, Sanofi, Bristol Myers Squibb, Pfizer and Genentech; and the Wellcome Sanger Institute. Generative AI has revolutionised the way we interact with knowledge. To more »
Worthing, England, United Kingdom Hybrid / WFH Options
Hobson Prior
Documentum and/or any other QMS systems. Acquaintance global GxP, e.g., FDA CFRs, EU, 'Third countries' other than the UK. Familiarity within a pharmaceutical manufacturing, testing or quality assurance setting in a similar position. Prior involvement with IT QA, maintained by knowledge of IT QA compliance needs and procedures more »
Prior of peptidome databases. Prior experience of analysing HLA- peptide presentation algorithms. A PhD in relevant subject, ideally with subsequent biotechnology and/or pharmaceutical industry experience. Ability to be present locally, nationally and internationally. Working proactively with the team to develop effective strategies prioritised to the needs of the more »
Slough, England, United Kingdom Hybrid / WFH Options
Parkside Recruitment
is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of more »
Stay updated on industry legislation and best practices. Act as a key member of the Quality Leadership team. Minimum Qualifications & Experience: Substantial experience in Pharmaceutical Manufacturing or Quality Assurance. Previous IT QA experience with familiarity in GxP IT systems. Proven ability in data integrity and systems validation. Strong communication and more »
level in science or equivalent experience. Minimum 5- 7 years of experience in the Regulatory Affairs regulatory experience with new product introduction within the pharmaceutical industry covering both UK National and European regulations Strong communication and project management skills Proficiency in the use of MS Office suite (Excel, PowerPoint) Ability more »
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 15,000 staff more »
or equivalent work experience supporting pharmacovigilance activities Proven experience as an IT Product Manager, preferably in an R&D or technology-driven environment or pharmaceutical industry Strong understanding of software development processes, agile methodologies, and IT project management. Excellent analytical and problem-solving skills, with the ability to translate R more »
experience to support our R&D business. Proven experience as an IT Product Manager, preferably in an R&D or technology-driven environment or pharmaceutical industry Strong understanding of software development processes, agile methodologies, and IT project management. Excellent analytical and problem-solving skills, with the ability to translate R more »
Brentford, Middlesex, United Kingdom Hybrid / WFH Options
GlaxoSmithKline
development processes, and ensure efficient deployment and monitoringPreferred Qualifications/Experience:If you have the following characteristics, it would be a plus:Understanding of pharmaceutical industry data and domain knowledge within CMC.Knowledge of GxP compliance requirements and experience implementing them in data engineering projectsPlease take a copy of the Job more »
Milton Keynes, Buckinghamshire, South East, United Kingdom Hybrid / WFH Options
Insite Public Practice Recruitment
k for 6 Months, Milton Keynes An exceptional 6-month contract opportunity has arisen with a leading innovative pharmaceuticals business that pioneers quality pharmaceutical products across the EMEA region. They are seeking a qualified Interim FP&A lead to join their renowned Product and R&D divisions. In this pivotal more »
Computer Systems Validation methodology as defined by QMS (global I&T Quality Management System) Required experience: 8 years relevant IT experience including specific experience Pharmaceutical/Biotech or similarly regulated environment experience is preferred. Deep understanding of and practical experience in Microsoft Collaboration and productivity tools, including but not limited more »
Leatherhead, Surrey, South East Hybrid / WFH Options
Client Server
be joining a SaaS technology scale-up within the HealthTech space that provides a range of trusted medical information to a range of Heath, Pharmaceutical and Life Sciences organisations. As a Senior QA Test Engineer you will take ownership of establishing Automated Test practices, processes and standards to support Agile more »
Leatherhead, Surrey, South East Hybrid / WFH Options
Client Server
be joining a SaaS technology scale-up within the HealthTech space that provides a range of trusted medical information to a range of Heath, Pharmaceutical and Life Sciences organisations. As a Senior Test Automation Engineer you will take ownership of establishing Automated Test practices, processes and standards to support Agile more »
PhD and/or MBA in the field of Biology, Biochemistry, or related Engineering is preferred.Advanced no of years of commercial experience in the Pharmaceutical, Biotech or CDMO space. Proven track record in delivering year on year financial and customer satisfaction targets. General understanding of drug development and commercialization pathways. more »
ExperienceMust have strong experience of working in Information Technology, especially the delivery and support of on-premise and cloud-based IT applications.Must have a Pharmaceutical backgroundMust have experience of Service Delivery and Service NowStrong skills in managing a diverse team of global staffExcellent interpersonal and communication skills with the ability more »
successful leader will be a dynamic, experienced individual with a strong track record of team leadership experience across various settings and topics in the pharmaceutical or biopharmaceutical industry. They should have the proven ability to lead a teamand manage complex projects effectively, influence stakeholders without authority, effectively network across the more »
can function properly. You will be working at GSK’s Worthing manufacturing facility where you’ll be learning how to maintain and improve our pharmaceutical manufacturing equipment and facilities, helping to ensure we can make the medicines and vaccines that we supply to patients. This is a 4 year practical more »
Bachelor's degree in Computer Science, Information Systems, or a related field. - Certifications in Tableau, Dataiku, SQL, or Python. -Prior experience working in a pharmaceutical company If you ae interested please apply or send your CV to luke.sandilands@cpl.com more »
Chesham, Buckinghamshire, South East Hybrid / WFH Options
Client Server
Developer you'll design and develop software to aid more rapid drug discovery for the Life Sciences and Pharmaceuticals industry; the product enables bio-pharmaceutical innovators to reduce manufacturing costs and ultimately expand patient access to vital drugs. Joining a collaborative Agile team as a Software Developer you will focus more »
our in-house training. Within the Analytical Sciences department in Sandwich, Kent we specialise in Material Sciences. We support our clients, primarily from the Pharmaceutical Industry, to shape drug product formulations, through defining safe and stable solid forms, investigating drug and excipients attributes, such as physical properties, thermal properties and more »
of conducting clinical studies of standard to high complexity and priority (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities more »
automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the more »
highly motivated ML researcher to join their team. You will be apply cutting-edge machine learning techniques, solving complex problems in the medical/pharmaceutical research field. Responsibilities Apply machine learning to solve complex problems Collaborate with a variety of scientific and engineering teams Develop software tools for internal and more »
