We are supporting a fast-growing

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Medical Devices company

that is developing innovative solutions. As the company continues to grow internationally, we are looking for a

QA/RA Manager

to take ownership of the Quality & Regulatory Affairs function and support the business in its next stage of expansion.

WHAT WILL YOU DO?
You will be the main point of contact for

Quality & Regulatory Affairs , working closely with the CEO and collaborating with Product, R&D;, Clinical, Marketing and Business teams.

Your responsibilities will include:
Lead and maintain the

ISO 13485 Quality Management System
Ensure compliance with

EU MDR 2017/745

and applicable medical device regulations
Manage Technical Documentation, regulatory changes and product compliance
Lead

PMS, vigilance, risk management, CAPA, non-conformities and change control
Coordinate audits and interactions with Notified Bodies and regulatory authorities
Support regulatory requirements for





international market expansion
Advise Product and R&D; teams on regulatory implications of new features and product changes
Review marketing claims and commercial materials from a regulatory perspective
Support the company in navigating the regulatory requirements associated with

software and AI

WHAT WE ARE LOOKING FOR?
•

5+ years of experience

in QA/RA within Medical Devices, SaMD, Digital Health or a similar regulated environment
Strong knowledge of

MDR 2017/745, ISO 13485 and ISO 14971
Experience with QMS, PMS, risk management, CAPA and technical documentation
Experience working with

Medical Device Software / SaMD

is highly valued
Experience with Notified Bodies and audits
Professional English and Fluent Spanish
High level of autonomy, ownership and attention to detail
Ability to work cross-functionally and translate regulatory requirements into practical business solutions

Nice to have:

IE

📌 RA&QA (Madrid)
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📍 Madrid