Skip to content
Apply now
MEDIVENA sp. z o.o.

Quality & Regulatory Affairs Manager (K/M)

MEDIVENA sp. z o.o. Show all offers
Warszawa
Lublin
Expires Oct 4, 2026
16 days ago

In short

Quality & Regulatory Affairs Manager in Warsaw for MEDIVENA. Responsibilities include QMS development, medical device registration, technical documentation, risk analysis, audits, CAPA, PMS, PMCF, vigilance, and training. Requires 3-5 years of QA/RA experience in medical devices, knowledge of MDR, FDA, ISO 13485/14971, and English. Remote work not available. Benefits: training subsidies, remote work option.

Keywords

ISO 13485 MDR FDA QMS audits CAPA PMS risk analysis medical devices ISO 14971

Summary written by AI from the data attached to this posting.

We collected this offer from another job board and only hold its basics.
Published 2026-09-04
Source

Hexjobs App

Tools tailored to this listing.