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 -
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 -
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 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 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 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
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
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 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 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