One of our growing sectors is supporting the hiring of Quality & Regulatory Affairs professionals, often with our Medical Devices and Pharmaceutical clients, but also in many of our High-Tech Engineering sectors who rely upon rigid and precise testing procedures before a product is fit for customers. When Supplier Quality is imperative, we recognise the necessity for experienced professionals.
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.
Candidates with GMP/GxP/ISO 13485 experience are in high demand and we have a broad and expansive database and network of impressive skillsets.
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 globally, 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.
Whether you are looking for a permanent addition to your team, or for somebody on a contract or temporary basis, we are able to rely upon our extensive database and network to provide you with outstanding, first-class professionals.
