Technical Documentation and Regulatory Affairs - Berlin, Deutschland - Hologic

Hologic

Geprüftes Unternehmen

Berlin, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

About us:

As a leading innovator of women's health, we at Hologic are empowering people to live healthier lives everywhere, every day.

Our quality and regulatory affairs team is responsible for keeping abreast of new, changing, and existing regulatory requirements.

They lead the development and implementation of a global vision for regulatory affairs, government relations, quality management and market access, to influence strategic and operational plans.

Tasks:

As the Technical Documentation and Regulatory Affairs Expert here at Somatex, part of the Hologic group of companies, you will be responsible for the creation and maintenance of technical documentation according to the relevant Medical Device Regulations.

Your responsibilities will include but are not limited to:

Creation and maintenance of technical documentation according to Medical Device Regulation 2017/74
Function as PRRC
Person Responsible for Regulatory Compliance according to Medical Device Regulation 2017/745 Article 15 regarding:

- preparing and keeping up to date the technical documentation and the EU Declaration of Conformity,

Communication with the notified body or authorized consultants on relevant topics
Collaboration in the maintenance and further development of the QM system according to DIN EN ISO 13485 as well as 21 CFR 820
Creation, maintenance, and revision of QM documents
Processing and followup of CAPAs

- support of international registration of medical devices in different countries