10 Contract jobs found in South East

Are you an experienced Labelling Lead? Do you have pharmaceutical or biotechnology regulatory experience, including regulatory labelling? If so, our Biotechnology client is looking for individuals just like you! The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our clients products for patients and healthcare providers glo

Are you an experienced EHS Manager? Do you have experience in providing direction to the delivery of EHS support/services in a multi-site, multi-division operation to ensure that business objectives are met? If so, we are keen to speak with individuals like you! We are recruiting for a Commercial EHS Manager to act as the EHS primary interface for our clients various sites as appropriate and advise them of necessary activities adhering to UK Law, HSE regul

Operations Test EngineerLocation: MK13 8PE, Milton KeynesSalary: £19.80- £24.10 per hour PAYEDuration: Initial 12 months The role: Exciting opportunity for a skilled Operations Test Engineer lasting over 12 months on a contract basis, assisting with the designs and implementation of test processes of components or products in a manufacturing environment.Duties/Responsibilities may include:Use of Vector & CanAnalyzer to communicate with battery pack & asso

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

Are you an experienced Regulatory Affairs Strategist? Are you interested in being the Regulatory Representative for assigned due diligences, under the direction of the Global Regulatory Strategy Lead? If so, our Biotechnology client is looking for individuals just like you!The successful candidate will be a member of a diligence team, responsible for contributing to the diligence on behalf of regulatory affairs and will be empowered to seek optimal strateg

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

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