1 to 25 of 717 Pharmaceutical Jobs

vast experience in M&A, IT and transformation services in the Life Science industry. Our current client base is predominantly in the Medtech and Pharma industry. Our team transforms complexity into priority actions, a clear timeline, and executive decisions supported by appropriate governance. You will be able to work with more »

across oncology, auto immune and cardiac therapy biomarkers, has helped deliver robust clinical data to expedite successful regulatory submissions and global market launches for pharma, laboratory and IVD clients, big and small. ARC Regulatory continues to create a reputation as a "Great Place to Work". Our commitment centres around more »

Job Description Senior Information Security Analyst Our Client is a leading global company specialising in pharma products. They are looking to recruit a Senior Information Security Analyst with at least 5 to 7 years expertise in Technology Security. The Senior Information Security Analyst is responsible for maintaining information security policies more »

Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. more »

various relevant Microsoft platforms, tools, technologies, patterns, and techniques related to Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. more »

About the Position : Location: Liverpool, England ( Onsite ) Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe more »

healthcare companies in the world to help support the production of dbDNA as a critical starting material for ATMP production and as an Active Pharmaceutical Ingredient. Touchlight is currently seeking an experienced scientist to join its Analytical Development department . This role, based at the Hampton site (UK), would be more »

Ariba and S/4HANA implementations. Experience Record to Report, I2P, RPM/PPM, SOA Manager, ABAP and WebMethods is a plus. Experience in Pharmaceutical Industry, is a plus. Demonstrated technical leadership experience. Understanding of Procurement business processes and Supplier master data. Knowledge of integration of S/4HANA Procurement more »

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 »

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 »

planning, time management and organizational skills. Experience demonstrating knowledge of essential regulatory guidelines world-wide. Awareness of or experience in clinical space in a pharmaceutical or biotech R&D environment or leading academic research center. Strong written/verbal communication skills and the demonstrated ability to work in a matrix more »

risks the systems present to regulated business processes To provide and or facilitate quality assurance oversight for the automation of business process associated with pharmaceutical manufacture and distribution To project problem identification/resolution/avoidance; typically involving ongoing interaction with management teams within Tech functions, site and local operating more »

RPi)To support the Head of Quality in ensuring the provisions of the licences are observed. Company Overview: Our client is a rapidly growing pharmaceutical wholesaling company involved in the procurement and supply of unlicensed medicines into the NHS and Private Hospital sector in the UK. They aim to deliver more »

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 »

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 »

integration of finance with other SAP areas like MM, PP, IM etc. Familiarity with data science concepts and use cases in Finance. Bio-Tech, Pharmaceutical or Life Sciences experience. Osirian Consulting is committed to working with our clients to promote equality and diversity in the workplace. We encourage and welcome more »

clearly demonstrated. Industry/domain skills: Extensive expertise in finance, HR, sales, marketing, product lifecycle management, manufacturing and post-sales service. Medical device or pharmaceutical industry experience is preferred. Experience in and understanding of a wide variety of analytical processes (governance, measurement, etc.). Experience with agile software development. A more »

and gene synthesis applications. Yourgene also has a global laboratory service network equipped to be a full life-cycle partner for clinical, research and pharmaceutical organisations to support partners at the preclinical, clinical, and post market stage to develop, manufacture, obtain regulatory approval and commercialise new products and services. In more »

A working knowledge of UK regulations is preferred. The candidate will be a convincing communicator with strong interpersonal skills. Previous experience working within the pharmaceutical sector will be advantageous. more »

Good networking and relationship building skills Desirable for the role: Experience of Commercial Finance and/or Group FP&A, preferably within a large pharmaceutical business Strong systems skills; advanced Microsoft Excel & PowerPoint, knowledge of Hyperion Planning would also be advantageous Why AstraZeneca? At AstraZeneca we’re dedicated to being 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 »

Dot is a cloud based, innovative software company and our product allows pharma and medical device customers to manage their quality processes electronically, replacing paper-based processes. We are looking for a Professional Services QMS Senior Project Manager, to join the leadership team of processional services and lead the technical more »

preventive actions as necessary. Qualifications: Bachelor's degree in a scientific discipline; advanced degree preferred. Extensive experience (10+ years) in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry, with a focus on the UK and Irish markets. Oncology experience is beneficial. Demonstrated expertise in UK and Irish regulatory 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 »