One of our growing sectors is supporting the hiring of Quality & Regulatory Affairs professionals, often with our Medical Devices and Pharmaceutical clients.
Probably the most critical part of the ‘journey’ to taking a product to the patient, these niche candidates are focused on delivering high-quality products to end-users, ensuring that products comply with strict government regulations.
Regulatory Affairs and Quality Assurance professionals have very different skill sets and here at The ONE Group, we recognise that. ‘Reg’ Affairs highlights adherence to legal regulations, while QA professionals focus on customer reception to final products.
We are fortunate to be able to support not only Pharma companies but also Medical Device companies through their journeys to getting products through regulations. We operate predominantly in the Cambridge area, but also nationally, and have even partnered with a Dallas, TX company, where we enjoyed a visit to see their HQ and learn more about their very unique product.
We also have very close relationships with Medical Research companies who have their products available for clinical research and studies.