Regulatory Manager – BiocidesPermanent role based in either in West Yorkshire or ManchesterOur client, a global organisation is currently recruiting for an experienced Regulatory Manager, based at its...
Regulatory Manager – Biocides / ChemicalsManchesterOur client, a global organisation is currently recruiting for an experienced Regulatory Manager, based at its Manchester site and reporting to the Se...
Job SummaryAre you passionate about making a difference to patients’ lives? Do you want to build a strong career within a company that excels in delivering high quality research? Why not let our clien...
...Regulatory Affairs, Research & Development, Finance/Accounting. External: Suppliers, Service Providers. If this interests you, please apply with your updated CV and our team will get in touch with you...
...Regulatory Affairs within a company committed to continuous improvement and global compliance? Do you want to be part of a collaborative team working with ISO13485 and MDSAP standards? If the answer i...
...regulatory, etc.) * Ensure all materials adhere to regulatory, compliance, and internal style / brand guidelines. * Mentor or coach more junior writers; review and refine their outputs. * Contribute t...
...regulatory documents received directly from our suppliers. Validating and releasing customer orders promptly and accurately. Drafting and uploading essential regulatory documents to the EU Commission ...
...Regulatory Affairs within the life sciences sector
...regulatory requirements. * Monitor quality performance using Key Quality Indicators and drive continuous improvement. * Participate in regulatory and client inspections, including managing follow-up a...
...Regulatory Affairs, Quality Assurance and Field Service Engineering sectors
...Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for Pharmaceutical for Human Use (ICH) GCP, G...
...Regulatory Affairs. Ensure processes comply with ISO 13485, FDA regulations, and other relevant standards. Lead root cause analysis and corrective/preventive actions (CAPA) for process-related issues....
...regulatory affairs, or a similar role, with demonstrable experience in managing quality management systems (ISO 9001) and environmental management systems (ISO 14001). Experience in planning, conducti...
...Regulatory Affairs Lead within CMC. This is for a global pharmaceutical company based in Cambridge. You will be responsible for RA CMC strategy and provision of RA CMC expertise across the Development...
Job SummaryAre you passionate about making a difference to patients’ lives? Do you want to build a strong career within a company that excels in delivering high quality research? Why not let our clien...