12 pharmaceutical jobs found in Luton, East of England

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working

Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -

Project Coordinator Location: Slough Full Time: 37.5 hours Weekly, 7.5 hours Daily Contract: 6 months, possible extension Salary: £17.02 PAYE Are you driven to succeed? Dependable, and a trouble shooter? Do you have the ability to build excellent relationships, manage projects and finances? If so, we want you to consider becoming part of a Global business leader in our industry; helping us drive our businesses growth by assisting with our upcoming proje

Position: Clinical Data AdministratorLocation: WitneyWorking Days: Mon-FriPay Rate: £30,000 Main Purpose of RoleThe primary objective of this role is to deliver high-quality and efficient data management support to Clinical Affairs, the Science Support Group, and other departments as needed.Main ResponsibilitiesPerform and oversee the upload and verification of data from multiple sources.Monitor the entry and migration of clinical data, collaborating with

Do you consider yourself to be strong at relationship and stakeholder management, with great communication skills? Are you able to work effectively, implementing procurement strategies that will deliver best value for the business? If so, we are looking for an individual who would be interested in joining a global medical device manufacturer as a supplier account manager. You will be responsible for a number of tasks from negotiation of commercial contrac

Are you an experienced Senior Scientist? Do you have experience in recombinant protein production? We are recruiting for a Senior Scientist to work within our clients Protein Production Group supporting projects from early stage target validation through to those undergoing pre-clinical evaluation, by generating recombinant protein reagents for immunisation, structural studies, assays and compound screening. All reagents produced undergo biophysical analys

Are you an experienced Senior Scientist? Do you have experience in sterile drug product development / manufacturing within the pharmaceutical industry? We are recruiting for a Senior Scientist to work within Drug Product Development establishing robust, fit for purpose biologicals drug product manufacturing processes for the different development phases. You will be defining and selecting drug product manufacturing processes and parameters for clinical man

Are you an experienced quality administrator or engineer? Do you have experience in managing multiple records from a document control and data entry point of view? We are recruiting for an Associate Quality Engineer to be accountable for supporting QA Engineers', Lead QA Engineers' and QA Managers' activities. This includes supporting the development and maintenance of their Quality System procedures for Design Control, Process Validation, Software Validat

Senior Agile Project Manager 6 Months FTC Pay: £60,000 Hours: 40 hrs per week, starting at 9 am UK time London, Hammersmith office A global client, who are leading the digital transformation of life sciences, are looking for a Senior Agile Project Manager/ Scrum Master to join on a Contract, developing cloud-based software solutions for clinical trials. You will also manage internal software development projects in a regulated & agile environment The

Do you have previous industrial experience in the area of drug discovery? Can you generate LC-HRMS metabolite profiling data from the analysis of in vitro & in vivo samples? We are recruiting for a Biotransformation Scientist to work for our clients Biotransformation & Enzymology Group. You will be providing cross-project support across a range of new chemical entities from early stage hit identification through to pre & post-clinical evaluation. As part o

One of our leading private healthcare clients are looking for a dynamic Procurement Manager to join their pathology team! With specific and high level laboratory experience the Procurement Manager will ensure best in class industry pricing and contract terms and conditions, whilst managing a small team to support our key stakeholder with the procurement of outsourced pathology services.Essential Experience required to be considered:*Laboratory Procurement