Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
Medical Science Liaison (MSL) - North TerritoryContract: 12 Months About This Role:You will be providing crucial medical and scientific expertise for a 12-month maternity leave cover. As an MSL, you will play a vital role in understanding disease products while forging valuable partnerships within the medical community and healthcare systems. Your contributions will significantly impact our company's success, both internally and externally, through medical
Medical Science Liaison (MSL) - North TerritoryContract: 12 Months About This Role:You will be providing crucial medical and scientific expertise for a 12-month maternity leave cover. As an MSL, you will play a vital role in understanding disease products while forging valuable partnerships within the medical community and healthcare systems. Your contributions will significantly impact our company's success, both internally and externally, through medical
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 -
Become part of our innovative team at Waltham and contribute to scientific breakthroughs that improve the lives of millions of pets worldwide. As a Bioscience Laboratory Scientist, you will execute a range of experimental techniques and methodologies with precision and technical expertise to advance research projects.Key Responsibilities:Execute various laboratory methodologies to generate high-quality data aligned with project objectives set by Senior Res
Become part of our innovative team at Waltham and contribute to scientific breakthroughs that improve the lives of millions of pets worldwide. As a Bioscience Laboratory Scientist, you will execute a range of experimental techniques and methodologies with precision and technical expertise to advance research projects.Key Responsibilities:Execute various laboratory methodologies to generate high-quality data aligned with project objectives set by Senior Res
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
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
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
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 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
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
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