Job Description

Quality and Regulatory Affairs Manager (m/f/d) – Medical Devices


Location: Hamburg or remote

Who we are

LITERO GmbH is a specialized consulting company supporting medical device manufacturers in meeting global quality and regulatory requirements. Our team provides expert guidance in quality management, regulatory compliance, and clinical affairs according to ISO 13485, IEC 62304, MDR, FDA, and other international standards. From developing and maintaining Quality Management Systems to preparing technical documentation and navigating global registrations, we help our clients bring safe, compliant, and innovative products to market.

Your responsibilities

Preparation and maintenance of quality management documentation according to ISO 13485 and related standards Preparation of regulatory documentation and support of submissions in line with MDR, FDA, and other international regulations Conducting regulatory gap analyses and supporting the integration of global requirements into client QMS Advising clients on product classification, conformity assessment, and international market access

Your profile

University degree in life sciences, engineering, medical technology, or a related field At least 2 years of professional experience in Quality and/or Regulatory Affairs for medical or pharmaceutical products Solid understanding of MDR, ISO 13485, ISO 14971, IEC 62304, and risk management processes Independent, structured, and proactive working style Fluent in English (German proficiency is a plus) What we offer Flexible and remote working options A small, supportive, and dynamic team Opportunities for professional growth and specialization Regular training programs 30 days of annual leave

If you are passionate about regulatory excellence and want to contribute to advancing safe and compliant medical devices, we look forward to receiving your application!


Apply by sending your CV: info@litero-agency.com

Daten

Art der Beschäftigung:

Stellenangebot

Befristung:

Unbefristet

Bereich:

Medizintechnik

Einsatzort:

Hamburg, Hamburg or Remote

Beginn:

02.01.2026

Wochenstunden:

Teil- oder Vollzeit

Kontakt

Unternehmen:

LITERO GmbH

Ansprechpartner:

Dr Kristijana Milovic-Holm

E-Mail:

k.milovic-holm@litero-agency.com