- We're seeking a Complaints Investigators to join our team at a leading global medical device and health care company based in Witney, Oxfordshire.What You'll Do:Investigate Product Returns: You'll play a crucial role in ensuring the highest quality standards by conducting thorough investigations into customer-returned products, meticulously identifying the root cause of any issues. (This is not a customer service role; you won't be handling customer calls!We're seeking a Complaints Investigators to join our team at a leading global medical device and health care company based in Witney, Oxfordshire.What You'll Do:Investigate Product Returns: You'll play a crucial role in ensuring the highest quality standards by conducting thorough investigations into customer-returned products, meticulously identifying the root cause of any issues. (This is not a customer service role; you won't be handling customer calls!
- ResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.ActResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.Act
- Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to undAre you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to und
- ResponsibilitiesEnsure training documentation is current and accessible; support overall LMS functionality.Coordinate issuance and reconciliation of documents and labels to meet production and project timelines.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global tResponsibilitiesEnsure training documentation is current and accessible; support overall LMS functionality.Coordinate issuance and reconciliation of documents and labels to meet production and project timelines.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global t
- Are you an experienced Senior Pharmacovigilance Scientist? Are you interested in overseeing and leading the process for safety signal management activities and aggregate reports? If so, we would love to speak with you. We are hiring for a Senior PV Scientist to join a globally leading Biotechnology client of ours, ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies areAre you an experienced Senior Pharmacovigilance Scientist? Are you interested in overseeing and leading the process for safety signal management activities and aggregate reports? If so, we would love to speak with you. We are hiring for a Senior PV Scientist to join a globally leading Biotechnology client of ours, ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are
- ResponsibilitiesCollaborate with system owners to design and maintain compliant, efficient quality systems supporting GMS and product lifecycle.Oversee data integrity and act as system administrator for key Quality Systems.Manage site Quality System Governance, ensuring compliance with company standards and regulatory requirements.Evaluate, approve, and monitor suppliers, including managing quality agreements.Lead change control processes and handle regulaResponsibilitiesCollaborate with system owners to design and maintain compliant, efficient quality systems supporting GMS and product lifecycle.Oversee data integrity and act as system administrator for key Quality Systems.Manage site Quality System Governance, ensuring compliance with company standards and regulatory requirements.Evaluate, approve, and monitor suppliers, including managing quality agreements.Lead change control processes and handle regula
- 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
