1 to 25 of 646 Pharmaceutical Jobs in the UK excluding London

computer software such as MS Word, MS PowerPoint, MS Project, and VisioEducation/Experience: PMI or PMP certification preferred Experience in project management,in pharmaceutical or related industries Experience with Software as a Service (SaaS) platformsAdditional Requirements: Collaborative mindset Open, honest, and transparent communication style Leadership qualities Client and stakeholder 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 »

leads and inspires colleagues. • Strong influencing and leadership skills. Understands influencing, stakeholder management and negotiation strategies. The Client is ideally seeking someone from a Pharmaceutical or Bio Science background and who understands how to work with the government and government funding. This position will manage 15 people within the IT more »

programme | Recognition awards | Free Parking Bespak Holmes Chapel is an Investors in People silver award winner who employs over 300 people and are a pharmaceutical Contract Development and Manufacturing Organization (CDMO) that offers development and manufacturing solutions for a variety of medical products. Our products include medical devices such as 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 »

and use of clinical data Experience leading projects with multiple stakeholders Experience of the use and management of Information within the NHS, academic or pharmaceutical community Extensive experience with Microsoft Word, Excel, PowerPoint, and Outlook Experience of documenting results for publication Experience of successfully managing a number of equally important more »

scientific or laboratory setting.Other key deliverables include: A proven track record of successfully designing and implementing a QMS within a Life Science Research environment, pharma or biotech. The ability to be adaptable to new challenges and changes within a company bringing a flexible approach to day-to-day operations. Strong 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 »

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 »

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 »

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 »

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 »

brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects more »

/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »

get stuff done” without an overreliance on process A self-starter with high levels of drive, energy, resilience Desirable Skills/Experience: Involvement in pharma IT and/or R&D/Commercial/Operations networks and organisations Experience of working with onshore and offshore suppliers Demonstrated understanding of quality 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 »

brands by working with them to find solutions which are operationally efficient, and drive profitability. We work across a range of sectors including Power, Pharmaceutical, Petrochemical, Oil & Gas, Food & Beverage, Bio Energy and Paper, but to name a few. We offer an end-to-end virtuous cycle approach to projects more »

units Ability to deliver high quality, consistent results in a timely fashion with a positive can-do and result oriented attitude Preferred Qualifications Extensive pharmaceutical or biotechnology industry research experience working on drug discovery project teams. Background of immunology Experience in flow cytometry A track record of scientific Publication Strong more »

with a positive can-do and result oriented attitude Prior experience of managing or supervising (more) junior members in a laboratory Preferred Qualifications Previous pharmaceutical or biotechnology industry research experience working on drug discovery project teams. Experience of flow cytometry A track record of scientific Publication Strong understanding of cancer more »

associated processes required to bring medicines to market such as; Explore, evaluate, and implement state-of-the art automation and digital technologies to support pharmaceutical process development, analytical and manufacturing workflows to improve efficiency, quality and processes and modernise capabilities. Develop, maintain, and validate laboratory software and computerised analytical equipment more »

Title: Automation Project Manager - Global Pharma Location: Near Watford Company Summary My client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. By joining my client, you will be working for an organisation with a human healthcare philosophy, which means … Desirable - Practical experience working on manufacturing execution systems (MES) OT Cybersecurity knowledge Experience working with edge computing/IIoT Practical experience working within the pharmaceutical industry Experience of serialisation/vision systems and interfaces to enterprise systems Practical experience working with Siemens PLCs and HMI software Experience of working with … pharma.co.uk If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/ more »