The Manager, Lead for Regulatory Affairs, Europe, will be a key team player working in a matrix with other PPTA staff to manage the regulatory and scientific affairs activities primarily in Europe. The manager will be responsible for evaluating and reporting on industry issues of a regulatory and scientific nature. This includes monitoring, evaluating, and contributing to legislative, regulatory, quality and safety initiatives related to plasma therapeutics industry, through working with PPTA’s members to develop consensus positions and guidelines to shape decisions of a range of stakeholders to improve the regulatory environment and, ultimately, the availability of PDMPs in Europe. The manager will maintain active collaboration with partner industry trade associations on issues of joint interest.
The application must include a CV, a cover letter outlining the motivation for this position at PPTA, and including a 1-pager outlining an overview of key regulatory issues and priorities of the plasma products industry in Europe. Please click here and follow the instructions carefully to attach your CV and cover letter.
The interviews for the position will take place in Brussels and/or online. In case of questions, please do not hesitate to send an e-mail to email@example.com.