- Are you an experienced Regulatory Affairs specialist or Medical Writer? Do you have experience in the writing / authoring of technical files? If so, we would love to speak with you! We are recruiting for a Regulatory Affairs Specialist to join our clients Infectious Disease business unit, preparing documentation for international product registrations. We are looking for someone with an RA or Medical Writing background, preferably within an IVD or medicaAre you an experienced Regulatory Affairs specialist or Medical Writer? Do you have experience in the writing / authoring of technical files? If so, we would love to speak with you! We are recruiting for a Regulatory Affairs Specialist to join our clients Infectious Disease business unit, preparing documentation for international product registrations. We are looking for someone with an RA or Medical Writing background, preferably within an IVD or medica
- Do you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainteDo you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainte
