1 to 25 of 619 Pharmaceutical Jobs in England

for the territory. Ophthalmic Hospital sales/Hospital formularies/CCGs or ICBs (product switches). To have an encyclopaedic knowledge of the Local Pharmaceutical and Medical Device market, its demographics, and customer profiles. Responsible for identifying key stakeholders and establishing relationships with influencers and decision-makers to facilitate broader … and affordability of eye care around the world. Qualifications: University degree (or equivalent) ABPI qualification Full UK driving licence The Person/Experience: Experienced pharmaceutical or medical device sales representative in Secondary care. Proven track record of achievement and improved personal and business performance. Experience of organising, running, recruiting for … are suitable for this position, please send a copy of your CV. Alternatively call the recruitment team at Chemistree Solutions Ltd. Chemistree is a pharmaceutical and healthcare recruitment specialist. more »

Chip models from idea to publication, with a focus on applications for safety testing to be used in drug discovery and development in the pharmaceutical industry. Conduct experiments using cell biology and bioengineering tools. Provide fully costed and planned projects and active use of project management tools to track budgets more »

and articulation of Amgen's positions on regulatory and R&D policies that impact Amgen's business. Key responsibilities: Master a range of bio-pharmaceutical R&D topics, ranging from digital health and precision medicines, through to patient centricity and geo-political uncertainty. Provide coverage of European regulatory issues pertaining … manager, able to coordinate the delivery of creative multi-channel communication programmes across different, yet interconnected policy topics. Related experience of working within bio-pharmaceutical, clinical diagnostics, life science sector is an advantage. Alternatively, experience of working within a compliance-led highly-regulated sector will be considered. Understand impact of … regulatory and R&D environment on all areas of the bio-pharmaceutical business, and actively seek synergies. Experience in government or a regulatory authority would be welcomed THRIVE What you can expect of us As we work to develop treatments that take care of others, so we work to care more »

commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. It’s our big vision that unites … of challenging and exciting projects. Essential in the role: MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) with experience in pharma/healthcare or other relevant area Knowledge of the technical and regulatory requirements related to the role Leadership capabilities to be able to lead and more »

functional team that works collaboratively with the platform and product engineering groups to implement and maintain real time process monitoring, informatics and modelling on Pharmaceutical Supply Chain (PSC) production and R&D Oral and Solid Dose (OSD) process platforms. The role is a key component for the long-term strategy … division’s Director (Oral Solid Dose MSAT), you will own and provide technical expertise for PAT and Modelling of production data with a One-Pharma team working in the R&D and manufacturing sites. Key elements of the role include: Managing the development of skills within a high performing team … capable in the regulatory guidelines applicable to the implementation of PAT within a manufacturing environment. Links/interactions with the regulatory authorities and other Pharmaceutical companies (to ensure that updates/new guidelines are fit for implementation across the Ware Campus) would be highly advantageous. About You: This role would more »

commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. It’s our big vision that unites … staff in the technical arena. Knowledge, Skills & Experience Required MSc/PhD in Statistics or Mathematics(containing a substantial statistical component) with experience in pharma/healthcare or other relevant area In depth knowledge of the technical and regulatory requirements related to the role Expert leadership capabilities to be able more »

commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. It’s our big vision that unites … regulations/developments in the area of Clinical Development and Biostatistics Appropriate experience as a statistician for the relevant position level with clinical trials, pharmaceutical development, regulated research, and/or related areas of statistical applications A collaborative mindset A general dedication to and ability to apply expertise to problem more »

commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. It’s our big vision that unites … regulations/developments in the area of Clinical Development and Biostatistics Appropriate experience as a statistician for the relevant position level with clinical trials, pharmaceutical development, regulated research, and/or related areas of statistical applications A collaborative mindset A general dedication to and ability to apply expertise to problem more »

related field, or equivalent. Have a compliance qualification (desirable) Have at least 3 years of experience within a corporate compliance function (ideally within a pharmaceutical or med-tech company) Have an in-depth knowledge of compliance, governance, risk and control frameworks within a corporate function Demonstrable experience, of developing and more »

QC Radiochemist/Analyst Working exclusively with an international advanced pharmaceutical company, I am currently supporting multiple hires within their QC team for one of the UK facilities based in South Yorkshire. These positions are hands on production scientists within a significantly growing area of radiopharmacy – however, no prior experience … shifts Must have own transport to access the site due to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

lovely global agency! The agency This full service events and comms agency work with well known global brands, predominantly in the automotive, technology and pharma sectors, to deliver a range of events and experiences. From large scale congresses for 1000's to stand alone meetings for 500 delegates, through to … supplier network and work in a collaborative way with all departments. Ideally experience working with Cvent and an understanding of the compliance in the pharma and life sciences industry is key to apply. If this sounds like you apply today! This one will go quickly! Get in touch with us more »

specialised experience in the Data Centre sector. As part of an expanding regional network, you'll join a company investing in new capabilities within Pharmaceutical and Defence verticals. This is a unique opportunity to be part of a quality-driven, financially robust organisation that values teamwork, innovation, and forging long more »

QC Radiochemist Join a dynamic team as a QC Radiochemist/Analyst at an esteemed international pharmaceutical company. The QC team is expanding at our client’s cutting-edge facility in South Yorkshire, UK, and we're seeking individuals from various experience levels, from graduates to seasoned professionals. In this … to adhere to regulated procedures Flexibility to work shifts If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below or contact Jolie Trahar for more information. Keywords: QC, quality control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry level, graduate, science, pharmaceutical, biotechnology more »

advanced understanding of SENISCA’s R&D capabilities and assets to identify, protect, market, and commercialise SENISCA’s intellectual property in the biotech and pharma sectors. Responsibilities include: Defining and implementing the Company’s IP strategy, ensuring that SENISCA’s IP strategy aligns with business goals, and overseeing the management … understanding of IP principles and a strong biopharmaceutical industry background in all major IP and licensing-related matters with experience in business development, handling pharmaceutical patent portfolios, and working with external patent attorneys. Strong core oligonucleotide and/or small molecule patent prosecution skills in multiple markets and jurisdictions. Experience … enterprise leader for the organization. Nice to have: Ph.D. level or equivalent in a relevant discipline. Significant industrial experience in biotech and/or pharma in developing either oligonucleotide and/or small molecule therapeutics; ideally both modalities. At least three years of relevant experience in life science patent prosecution more »

Here at EMIS, we have a truly exciting opportunity for you to join our highly capable and talented Community Pharmacy product team as a Product Manager on a permanent basis. Responsible providing essential technology to 5,8000 pharmacies across the more »

any quality related matter. Minimum Qualification (education, experience and/or training, required certifications): Scientific Degree or an equivalent in Chemistry, Biology, Pharmacy or Pharmaceutical Engineering; Min. 5 years of experience in quality operations in the GMP environment; Other languages are an asset; Knowledge and understanding of regulatory requirements; Good more »

Leading Consultancy - London - £50k – £65k The Company Our client is a genuinely global marketing intelligence consultancy working in partnership with almost all the top pharma/biotech companies providing insight and strategic direction across a vast range of therapeutic areas. They utilise big data and a variety of bespoke applications more »

Position: IT Project Manager Type: Contract Duration: 6 Month We've currently partnered with a global Pharmaceutical company, who are look for a manufacturing PM. This position will manage the execution of IT/OT Projects for 3 manufacturing sites in the UK. This is a full-time position, with … of the Manufacturing IT Team, reporting into the IT Automation Lead. This contract role will initially be until December 2024. Requirements: Data Integrity Knowledge Pharmaceutical Industry Experience (GxP) BMS, EMS and SCADA Systems Experience and Knowledge Knowledge of IT and OT areas Ability to understand complex application and OT asset … 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 »

assets in the fast-paced realm of engineering and technology? Do you thrive on the challenge of ensuring compliance within the intricate landscape of pharmaceutical research? If so, we have the perfect opportunity for you! Overview: As a Information Security Manager, you will play a pivotal role in fortifying my … s degree in information security, Computer Science, or related field (Master's degree preferred). Proven experience in information security management, preferably within the pharmaceutical or healthcare industry. In-depth knowledge of relevant regulatory frameworks, such as ISO, GDPR, HIPAA, and FDA regulations. Strong understanding of security technologies and methodologies more »

This is a level 8-9 role and is a permanenet opportunity. Location is flexible – West Cumbria, Warrington London or Oxfordshire. Hybrid working is available with 40% of time in an NDA office. The salary range is £70,550 to more »

Cognex Vision Systems for automation. This exciting opportunity is to work within a leading company in the bespoke packaging lines sector, specifically serving the Pharmaceutical & Medical industries. You will be joining a company who provide solutions for complete product lifecycles working with the latest in automation technology. Machine Vision Specialist … high-level language programming, ideally in VB.Net and C#.Net Our client is a well-established business in the bespoke packaging lines sector for the Pharmaceutical & Medical industries. They are currently busy with high-technology projects and are looking for a machine vision expert to join their automation team. Travel is more »

Job Description This is a key role in providing essential service plans to our customers and their sites, reacting to various technical faults and planned maintenance of our products. Reporting to the Service Manager, in this role you will be 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 »

A degree in computer science, information technology, or a relevant technical field At least 6+ years of scrum master experience, preferably in a similarly sized global business Experience in traditional IT project management and hybrid delivery models Expertise in Agile more »