1 to 25 of 41 Permanent Biopharmaceutical Jobs in the UK

a Biopharma Downstream Process Development Scientist, R&D. ROLE: This is an exciting opportunity to join dynamic process team responsible for development of new biopharmaceutical and vaccine products. The Biopharma large molecule technical development team works collaboratively with an inclusive culture to deliver innovation. CANDIDATE: • Degree or higher degree within more »

approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects in the pharmaceutical and/or biopharmaceutical sectors. Working with other departments and key stakeholders Good communication skills and be proactive Successful candidates will be able to demonstrate technical competence, will be more »

and substantial experience in cell culture, specifically embryonic stem cells (ESC) and induced pluripotent stem cells (iPSC) culture and differentiation. Manufacturing Experience: Background in biopharmaceutical or cell and/or gene therapy manufacturing processes. Independence and Support: Self-motivated with the ability to work independently while effectively supporting team members more »

and resolve issues. Role Requirements: BSc or MSC in a life science subject or comparable experience Experience leading validation/qualification activities within the biopharmaceutical ATMP or related sector (e.g cleanrooms, production/lab equipment, monitoring systems) Clear working experience of generation and execution of validation lifecycle documents in adherence more »

Software Technical Lead - Control Systems Location: Chesterfield Rate: up to £60/hr - outside IR35. Our client is a leading engineering and maintenance provider, supporting customers across the chemical & petrochemical, nuclear, oil & gas, pharmaceuticals & biopharma, power & energy, utilities, renewables and more »

Belcan have joined forces with a leading engineering and maintenance provider, supporting customers across the chemical & petrochemical, nuclear, oil & gas, pharmaceuticals & biopharma, renewables, and food & beverage markets. They are looking to add to their workforce with an exciting opportunity for more »

The Opportunity: You will joining a global biopharmaceutical specialist to help prepare and manage the reliable delivery of IT systems in readiness for commercial launches, on time and to budget and meeting agreed quality criteria. The key systems enabling these launches are their Salesforce.com based solutions and Oracle based ERP. more »

on +44 20 3319 3199 or J.pawl@proclinical.com . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. more »

Responsibilities: Responsible for Daily Management of the Functional team and their performance; Leads people using company values and core behaviors with a GEMBA presence. Maintain Quality Management System in accordance with Corporate, BU and regulatory requirements advocating complainant change management. more »

delivery of software solutions. Manage the risk to avoid the need to test. Experience : Experience in quality assurance or software testing roles within the biopharmaceutical, pharmaceutical, or healthcare IT industry Profound understanding of software development lifecycle (SDLC) methodologies, quality assurance principles, and regulatory standards applicable to the biopharmaceutical sector. Proven more »

My client has a growing diverse portfolio of life sciences and diagnostic products for the pharma, biopharma, healthcare and environmental markets. Your role will involve finding new customers, building solid partnerships, and boosting sales through strategic selling. You will need more »

Ingenii Search are currently seeking a highly motivated Senior Product Manager to lead a dynamic team in the biopharma industry. As a Senior Product Manager, you will be responsible for driving the development and implementation of innovative software solutions that more »

any questions, please contact Ingrid Aymes at i.aymes@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. Proclinical Staffing is an equal opportunity employer. more »

the quality of IT services. Requirements Experience with quality management systems particularly Veeva Vault Understanding of the Quality area, data and processes within the biopharmaceutical industry Strong problem resolution, negotiation, and influencing skills Experience with agile development methodologies To apply please submit your application on Linkedin or alternatively email ahill more »

high motivation and high energy level, self-starter. For further details, please contact Larry on +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 more »

utilities and processes, including the generation of lifecycle documents (URS, DQ, IQ, OQ & PQ) in a biopharmaceutical. Significant experience leading validation activities within the biopharmaceutical or ATMP sectors Understanding and experience of aseptic processing and cleanroom technologies Proven track record of establishing validation master plans (VMPs) Apply : It is essential more »

therapeutic pipeline targeting specific age-related diseases with clear unmet medical need. The role presents an excellent opportunity for a dynamic individual with significant biopharmaceutical experience in patent portfolio management, the development and implementation of intellectual property (IP) and licensing strategies and the capability to lead our industry-specific relationships … diligence on business development opportunities and support licensing and strategic partnering activities. You’ll have: A demonstrated 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. more »

Title: Project Management Consultant Position Type: Contract OTS Location: Central London Categories: Project Management, Engineering PM Group requires a project manager with experience of biopharmaceutical projects to lead a client team in Central London. Responsibilities · Ensuring that the projects are delivered on time and within budget. · Presenting business cases, seeking … Reporting project progress against established milestones. · Other responsibilities in-keeping with the project management role. Qualifications Applicants will have experience of managing top tier biopharmaceutical projects from inception to completion and handover. The successful candidate will be able to communicate clearly at all levels (including interpreting and explaining complex technical more »

any questions, please contact Ingrid Aymes on I.aymes@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. more »

attention to detail is required. Proficient in Word, Excel and PowerPoint. Please contact Larry on +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 more »

Knowledge of engineering principles for scaling up and down of bioprocess operations. - Understanding of how to develop and optimise processes for the purification of biopharmaceutical products. - Understanding of GMP and QbD considerations in a large scale manufacturing environment. - Understanding and experience with statistical and modelling software and tools. - Understanding of more »

application 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 more »

validation requirements for computerised systems projects. Assist in the authoring of User Requirement Specifications. Experience: Sufficient prior experience of validating computer systems in a Biopharmaceutical setting. A Degree (or equivalent experience) in a Science or related discipline . Experience in the validation of GxP software and Laboratory systems. Prior ERP more »

candidate must have the right to work in the UK. Our Benefits Our goal is to simplify progress in life science research and the biopharmaceutical industry, translating scientific findings into new therapeutics more efficiently, so that more people can access better medicine. With nearly 11,000 employees at over more »

Our Client is a leading biopharmaceutical company dedicated to discovering, developing, and delivering innovative therapies that improve the lives of patients. Their commitment to excellence is reflected in our pioneering research, groundbreaking treatments, and unwavering dedication to quality and compliance for innovative medicines. Position Summary: The Regulatory CMC Development Associate more »