Laura Taylor Featured Image

Laura Taylor

BSc MSc

Senior Manager

Regulatory Affairs Medical Technology

Laura has worked in regulatory affairs since 2015 specifically in the medical device industry. She has experience with regulatory affairs, medical writing, quality management systems, and auditing.

She has previously worked for an orthopaedic medical device manufacturer with products sold globally. In her previous position, she specialised in quality management systems, medical writing including technical files and clinical evaluations reports, risk analysis, management of post market surveillance and CE marking medical devices, from Class I through to Class IIb implantable. As well as managing Notified Body audits covering Medical Device Directive, Medical Device Regulation, ISO 13485, UKCA, MDSAP markets, FDA CFR 820 and Canadian Medical Devices Regulations.

Whilst employed by tranScrip, Laura has also worked on medical devices related to wound care, sexual health, gastrointestinal health, as well as providing support with medical writing activities for pharmaceutical products and management of pharmaceutical product registrations.

Prior to making the move to the medical device industry, Laura worked in quality management for a UK university. She has a degree in life Sciences (BSc) and post-graduate master’s degree (MSc) in Strategic Quality Management.

Laura is also a certified Lead Auditor for ISO 13485:2016 – Medical Devices – Quality management systems – Requirements for regulatory purposes. She is also a member of European Medical Writers Association (EMWA).

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Our experienced physicians and scientists, together with our regulatory, clinical and commercial experts can support you to maximise the value of your products. Whatever your project requires, we have the expertise to meet your needs.