Rebecca Rutter

Rebecca Rutter is a UK Qualified Person and senior executive quality leader who brings over two decades of pharmaceutical and life sciences experience to TDP's most complex client engagements. Her background includes eight years at GSK in senior roles spanning Director of Manufacturing for Cell and Gene Therapy, Global Quality Lead for Consumer Health, and Category and R&D Site Quality Manager. That experience of quality leadership at the highest level within a global pharmaceutical organisation gives TDP clients access to strategic and technical insight that is exceptionally difficult to find.

Rebecca's specialist expertise within TDP covers ATMPs, sterile and aseptic manufacturing, and the design and commissioning of GMP facilities. She has been involved in the set-up and decommissioning of three ATMP and biologics GMP facilities in the UK, including a greenfield site build, experience that gives TDP a genuine capability in full facility lifecycle support that few consultancies can offer. Her approach as a QP is grounded in the principle that good decisions at every level must be made with scientific rigour and clear risk understanding, with the entire supply chain and the people within it considered.

At TDP, Rebecca provides senior QP services and strategic quality leadership for clients operating in some of the most technically demanding areas of the industry. Her combination of executive-level experience and deep technical specialism in ATMPs and sterile manufacturing makes her a significant asset for clients where the stakes are high and the regulatory complexity is considerable.