CSV Engineer

We are seeking a motivated CSV Engineer to join our team. The ideal candidate will be responsible for ensuring that computerized systems are validated in compliance with industry regulations (GxP, FDA 21 CFR Part 11, EU Annex 11) and internal company procedures.

Responsibilities
:

Develop, review, and execute validation documentation (URS, FS, DS, IQ, OQ, PQ, traceability matrices, validation reports, etc.
)Ensure systems’ compliance with applicable regulatory requirement
sParticipate in risk assessments and define validation strategie
sProvide expertise and support during internal and external audit
sLiaise with Quality, IT, and business teams to coordinate validation activitie
sMonitor and maintain validated state of computer systems over their life cycl
eTrain end-users on relevant procedures and systems, if require

d
Qualification
s:

Bachelor’s or Master’s degree in Life Sciences, Engineering, Computer Science, or related fie
ld Prior experience in computer system validation, preferably in regulated industries (pharma/biotech/medical device
s)
Strong understanding of GxP guidelines and relevant regulations (e.g., 21 CFR Part 11, Annex 1
1)

Experience with validation of laboratory, manufacturing, or quality syste
ms Excellent documentation, organizational, and communication skil
ls Ability to work on multiple projects simultaneously and as part of a te
am Fluency in Engli

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