126 to 150 of 222 Pharmaceutical Jobs with Hybrid or WFH Options

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 »

Job summary We are excited to offer the opportunity to bring on board a Junior User Research Officer. As a digital team we are continuing to expand our growing team. As a User Research Officer you will be responsible for 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 »

Employer LGC LIMITED LGC Group is a global leader in the life science tools sector, providing mission critical components to customers across clinical diagnostics, pharmaceutical, research & government, food and other applied markets. LGC is an international life sciences company working with customers in the government, academic, pharmaceutical, agricultural biotechnology, food 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 »

Job summary This post is fixed term/secondment for 12 months for Maternity cover. If you are interested in applying for the secondment position, you must obtain permission from your current line manager prior to applying for this post. 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 »

Senior Automation Engineer | Contract | Pharmaceutical Plant | UK Position for a Senior Automation Engineer looking for a project-based role where you will support the overall delivery of DeltaV workstream at a leading pharmaceutical manufacture. The Senior Automation Engineer will work closely with systems integrators and engineering vendors to ensure all … deliverables meet project needs and liaise with senior stakeholders to ensure clear lines of communication. Our client is a leading global pharmaceutical organisation that is investing heavily across the site, and the projects include upgrade, and a high-value greenfield project. As NES Fircroft continues to support our clients across … software, software, hardware, system software, system hardware, automated production equipment, cGMP, cGMP environment, GMP, Good Manufacturing Practices, Manufacturing, Switzerland, Ireland, UK, Netherlands, Austria, Biopharmaceutical, pharmaceutical, GMP environment, sterile manufacturing, API, aseptic processing, Electrical engineering, pharmaceutical manufacturing, capital investment, project management, Automaton Manager, Automation Project Manager, Project Manager, Senior Automation Manager more »

Senior Statistical Programmer | Pharma | Fully Home Based | UK | Warman O’Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior Statistical Programmers to join them. This is an exciting time to join this inspiring place to work … will need: Bachelor’s degree or equivalent in Mathematics, Statistics, Data science/analytics, or other relevant scientific. Previous Statistical Programming experience within the pharmaceutical industry essential. Excellent knowledge of SAS essential and R or Python advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical more »

Project Manager | Permanent | Hybrid - Oxford | Circa £65k We are currently working on a new Project manager position at a super exciting pharmaceutical startup client based in Oxford. They are looking for someone to come and drive Good Clinical Practice (GCP) principles, who can come in and build relationships with key … stakeholders in order to keep the quality team moving forward. The ideal person will have strong QA experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup environment. This individual will also be a fantastic communicator, comfortable … key stakeholders across the business Report up to senior leadership and represent QA in reporting What you will bring: Previous project management experience within pharma/biotech or similar Outstanding knowledge of GCP, TFA and FDA regulations Strong project management principles, key knowledge of agile methodology A desire to be more »

Hours : 37.5 hours per week Salary : Competitive Ref No : HRJOB9568 Business Unit : Pharma Services Location : Loughborough, Leicestershire Open To : Internal and external candidates Please note this is a re-advertisement, if you have applied for this position within the past 6 months, we will be unable to accept your application … would also be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in a scientific or technical discipline Worked within a pharmaceutical/GxP environment in a Quality related role Familiarity with the production of solid dose oral products Management of electronic & physical documentation systems Reward For more »

business goals and objectives. Proven ability of accurate and timely completion of tasks. Educated to Degree level (or equivalent qualification) in Chemistry, Biology, Pharmacy, Pharmaceutical Science, Life Science, or comparable discipline. Ability to multi-task, set priorities and meet strict deadlines. Using logic and reasoning to identify solutions to problems. … First class organisational skills. Self-motivated, with the ability to work proactively using own initiative. At least 10 years of experience in pharmaceutical industry with hands on experience in or supporting operations. Experience of auditing quality systems/manufacturing/releasing for a variety of pharmaceutical dosage forms (including aseptic more »

/Engineering Project Manager Experienced Project Manager or Project Engineer with Validation experience? Read on. I am working exclusively with a multi-site advanced pharmaceutical company that are looking to expand their Projects team due to continued developments and also the prospect of new sites being introduced over the next … management team, you genuinely have the chance to control your own time and project management – therefore previous experience in managing engineering projects within the pharmaceutical setting is key. Given the plans for the business, the scope for further development and progression is significant. As well as a strong package, a … company car/car allowance will be offered as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk more »

Requirements for Lead Trial Master File Expert: Bachelor of Science degree is preferred. 10+ years’ experience managing TMFs in Clinical Operations environment, in the pharmaceutical, biotech or CRO industry working ICH/GCP guidelines. Experience in both paper and electronic TMF, and familiarity with naming and filing conventions and the … +353 1 – 2302400/larry@rftgroup.ie The RFT Group , BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie Follow us on Twitter, Facebook and LinkedIn more »