101 to 125 of 202 Permanent Pharmaceutical Jobs with Hybrid or WFH Options

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

an integrated provider. Trusted as compliance partners, we collaborate with clients in sectors such as Education, Health, Care Homes, Public Sector, Local Authority, Industry, Pharmaceutical, Hospitality, Leisure, Food & Beverage, Retail, and Media, to ensure risk reduction, safety improvement, and regulatory compliance. more »

in London or those interested in remote work from Turkey as we are looking for a medical writer who has expertise in healthcare and pharmaceutical industries by translating complex scientific and clinical information into clear and concise documents. Their primary responsibility is to communicate medical and scientific information to various more »

Basic informationLocationBristol, London, ManchesterService lineAudit & AssuranceDate published15-May-2024Req #15746Job descriptionConnect to your IndustryOur Assurance practice encompasses skills across regulation and finance with a deep analytics capability. We harness these to provide Assurance to those charged with governance, serving the more »

Basic informationLocationBristol, London, ManchesterService lineAudit & AssuranceDate published15-May-2024Req #15746Job descriptionConnect to your IndustryOur Assurance practice encompasses skills across regulation and finance with a deep analytics capability. We harness these to provide Assurance to those charged with governance, serving the more »

a life sciences discipline such as chemistry, biochemistry, bioinformatics, or similar with a strong computational element A track record of drug discovery within a pharmaceutical, biotech or contract research/CRO company or similar, preferably as a project leader Deep hands-on expertise of applying both structure-based and ligand … positions available. Keywords: computational, chemistry, modelling, hit, lead, structure, ligand, homology, quantum, QMMM, molecular, dynamics, protein, degradation, data, manager, computer, science, drug, discovery, biotech, pharma, lab, pharmaceutical, python, R, senior, lead, R&D, research, preclinical more »

Our Client develops and distributes innovative, high-value specialty pharmaceutical products. They are now seeking a Technical Specialist - Pharmaceutical QC and Manufacturing. This position is a full-time permanent role which will be office based in Surrey with blended (hybrid) working arrangements currently in place. Job Purpose Take day-to … current project process (trackers, classification of files etc.). Qualifications/Experience BSc or equivalent science-based degree Prior experience of working in a Pharmaceutical production or development environment, to include QC and working with staff on issues arising within a production environment. Familiar with the concepts of GxP systems … and other pharmaceutical terms and acronyms. Experience of managing Tech transfers, troubleshooting and product development of product change projects including process, analytical, planning, documentation, cost control and communication. Experience or ability to fill eCTD module 3. Ability to establish and maintain effective working relationships with internal and external stakeholders. Strong more »

do business. This role can be performed remotely in US, UK and any European Dechra entity. The Opportunity Dechra is an international specialist veterinary pharmaceutical products business. Our expertise is in the development, manufacture, sales and marketing of high quality products exclusively for veterinarians worldwide. The Director Quality CMC Development … inclusive employer and we embrace candidates from all walks of life. We're particularly keen to hear from those who have/are: Extensive Pharmaceutical Industry with hands on experience in development/quality in a GxP environment. Proven track record of implementing phase appropriate quality strategies Direct experience proving … priorities with aggressive timelines. High impact and influencing skills. Desirable Qualifications: Bachelor's, Master's Degree, or PhD in a relevant field - chemistry, pharmacy, pharmaceutical science, biology, life science, or comparable discipline. Additional Information: Extensive travel is essential for this role All applications received are reviewed by our internal talent more »

companies in Europe. This is a replacement role for someone who has been promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who … with some auditing experience. The role is based from home and will involve some travel. We require someone who has worked either for a Pharmaceutical company or a Facilities management company on site at a Pharma client. This role is focusing on the quality side of things and you will … background in managing compliance, experience of QMS and be able to conduct investigations around CAPA. Three direct reports 30% travel Client is a large pharmaceutical/life science company. Job purpose Provide oversight and regional strategic leadership across quality, safety, health, environment, risk management and business continuity throughout the EMEA more »

cybersecurity. Headquartered in Chesterfield, Derbyshire, with over 300 B2B customers, the Company works on cutting-edge projects in high-end food and beverage manufacturing, pharma, and energy. We are currently seeking experienced Digital Manufacturing/Automation Engineers (3+ years of experience) to manage and lead technical activities on digital manufacturing … Profibus, Modbus, DeviceNet). Knowledge of process instrumentation and wiring would be desirable. Experience working with validated Digital Manufacturing/Automation systems in the Pharmaceutical or Food Beverage manufacturing environment. Characteristics We look for candidates who Work well as part of a team. Have excellent problem solving and diagnostic skills. more »

cybersecurity. Headquartered in Chesterfield, Derbyshire, with over 300 B2B customers, the Company works on cutting-edge projects in high-end food and beverage manufacturing, pharma, and energy. We are currently seeking experienced Digital Manufacturing Engineers (3+ years of experience) to manage and lead technical activities on digital manufacturing and automation … PLC Programming/HMI/SCADA experience desirable: Siemens, Rockwell, Schneider, etc. Experience working with validated Automation systems in the Food and Beverage or Pharma manufacturing environment. Characteristics We look for candidates who Work well as part of a team. Have excellent problem solving and diagnostic skills. Can prioritise and more »

IGES UK Pharma Ltd. is a new entity in the UK, and part of the IGES Group , set up specifically to offer strategic advice to clients for early trial planning and launch of new innovative medicines within the NHS system to secure reimbursement. In total, the IGES Group employs more … In collaboration with the wider IGES Group , the vision of the company is to provide a full service from strategy to submission for the pharmaceutical and biotech sector. As such the consultant has a vital role to lead client engagements through excellent communication, project management, and presentation skills. Besides, the … the company. Primary Responsibility: project delivery and Business Development activities in the Market Access space for existing and new named UK-local accounts of pharmaceutical and Biotech companies, working closely with the Director, and colleagues with delivery expertise in other functional areas and work closely with the Director on Business more »

come. You’re a healthcare guru : Passion for working in healthcare and experience working with healthcare clients and knowledge of the regulations in the Pharma Industry is essential. Understanding what can and cannot be done on social media and other digital platforms, both in the UK, Europe, and worldwide, and … What you should have: Up to 7 years of experience in digital/social media, with some of this served in health, biotech, or pharmaceutical media sectors. Agency experience required. College degree (BA or equivalent). A relevant concentration such as Marketing, Communications, Science, or a master's degree is … Excel Comprehensive understanding of the primary regulatory bodies (such as ABPI, PMCPA, FDA, and FTC) and the social media guidelines that govern biotech and pharmaceutical clients. Ability to grow digital and social media business (with current social, PR or marketing clients) and participate in new business pitches. Working with HART more »

R&D, a priority area for Veeva. We work with senior customer stakeholders, as the partner of choice for 85% of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance).As a Senior … degree and excellent academic record4+ years consulting experience in an established strategic/management consulting organizationExperience in Life SciencesGood understanding and deep interest in pharmaceutical R&D, having delivered consulting engagements in one or more of the following areas: Regulatory, Clinical, Quality, Safety.Good understanding of the R&D value chain more »

The chemical biology team at EMBL-EBI delivers world-leading databases and resources to the scientific community. Our flagship resource, ChEMBL , is a database of high-quality quantitative small-molecule bioactivity data curated from the scientific literature and direct data more »

The chemical biology team at EMBL-EBI delivers world-leading databases and resources to the scientific community. Our flagship resource, ChEMBL , is a database of high-quality quantitative small-molecule bioactivity data curated from the scientific literature and direct data more »

German 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 »

around at least one of: late stage/preclinical R&D, clinical studies, CMC, late stage development/commercialisation of drug candidates within the pharmaceutical, biotech or CRO industry A BSc (or equivalent experience) within a life sciences or business discipline, ec biology, chemistry, etc Excellent understanding of project and … your career. Keywords: PMO, project, program, programme, manager, management, R&D, clinical, research, trial, drug, development, preclinical, CMC, regulatory, business, launch, leadership, delivery, biotech, pharmaceutical, CRO more »

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world. We are currently 1,100 people … handover to BAU operations. Experience with regulatory compliance issues, as well as best practices in application and network security. Experience of working in the pharmaceutical or similarly regulated markets is desirable. Willing and able to travel in the UK as required. Willing and able to occasionally work outside core hours more »

An exceptional opportunity awaits with our client, a dynamic Regulatory Affairs Consultancy with a presence in the UK, Switzerland, and Ireland, serving global clients. In this role, you will join a team of seasoned experts in Regulatory, CMC, Clinical, and more »

At Mace, our purpose is to redefine the boundaries of ambition. We believe in creating places that are responsible, bringing transformative impact to our people, communities and societies across the globe. To learn more about our purpose, culture, and priorities more »