Regulatory Affairs Specialist
Vor 3 Tagen
Regulatory Affairs Specialist - Medical Device Manufacturing Project (Bavaria )
We're hiring
Regulatory Affairs Specialists
for a major
medical device manufacturing project
based in
Bavaria, Germany
Join a leading
Medical Device Company
in a
hybrid role
supporting regulatory submissions, compliance activities, and alignment with EU and international medical device regulations.
Location:
Bavaria (hybrid)
Duration:
12-month contract
Start:
ASAP
Key Requirements:
- Proven experience in
regulatory affairs
within
medical equipment manufacturing companies - Strong knowledge of
EU MDR
,
ISO 13485
, and familiarity with
FDA 21 CFR Part 820
is a plus - Skilled in preparing and reviewing
technical documentation
,
regulatory submissions
, and supporting
Notified Body interactions - Detail-oriented, proactive, and collaborative professionals preferred
If you're available and interested, please send your
CV
along with your
availability
. First batch of submissions goes out
today
-
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