H&T Presspart is pleased to announce further growth in our Global Quality Assurance & Regulatory Affairs team with the appointment of Rebecca Field as Regulatory Affairs Specialist.

Rebecca has a wealth of knowledge in Regulatory Affairs including Medical Device Regulations, Quality management and auditing of ISO Standards and Regulations in both Manufacturer and Supplies Facilities, as well as extensive experience of Regulators globally, particularly the FDA.

Following the recent purchase of our new manufacturing facility in Switzerland, H&T Presspart Nidau, the growth of our Global Quality Assurance & Regulatory Affairs team is key to support H&T Presspart’s strategic goals in the medical device contract manufacturing market as well as supporting opportunities in new markets such as ocular drug delivery and femtech.

Rebecca will report to Thomas Mitchell Director, Global Quality Assurance and Regulatory Affairs, and will be based at our site in Blackburn. We would like to welcome Rebecca to H&T Presspart and wish her all the best in her new role.