Hi,
Title:
Packaging Engineer (R&D) Onsite-Medical
Device
Location: Columbus, NE
Duration: 6+
months
NEED Genuine
and real time experience.
JD:
- Rich
experience as a package development engineer or a strong understanding of
the package development process and responsibilities
- Working
knowledge of 21CFR Part 820 & EU MDR -745/2017 regulations, as well as
the requirement of Medical Device packaging standards per ISO11607-1 &
2.
- Expertise
in Package qualification by performing various design verification
testings’ such as Package integrity, Seal strength, Microbial barrier, Ink
Legibility & Performance, Box compression, Label Adhesion and Ship
tests etc., for disposable medical devices (hypodermic syringes, needles
etc...) Per ISO 11607 in accordance with ISO 13485 / US FDA 21CFR part820
requirement.
- Extensive
knowledge on Medical Device packaging shipping container distribution test
requirements per ASTM 4169/ ISTA standards
- Exposure
to various sterilization techniques and experienced in sterilization
requirements for various medical device-packaging materials.
Thanks & Regards,
Andy
Saibber
And...@Saibber108.com
T: 717-610-1199 Extn 431
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