GMP Validation Specialist (IQ/OQ/PQ)

ProductLife Group

Emilia-Romagna

In loco

EUR 34.000 - 39.000

Tempo pieno

42 ore fa

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Generatore di candidature

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Descrizione del lavoro

ProductLife Group in Italy is seeking a Validation Engineer to execute and document calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment, and to prepare validation protocols and reports in compliance with GMP.

The role requires 3–4 years of experience, a bachelor’s degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related discipline, and professional English and Italian language skills; travel to client sites may be necessary.

Competenze

3–4 years of experience in validation or related field.
Experience drafting qualification protocols, reports, SOPs, and GMP documentation.
Good understanding of GMP requirements and validation principles.

Mansioni

Execute and document calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment.
Prepare validation protocols, reports and related documentation.
Support change controls, deviations, CAPAs, and risk assessments related to validation.
Collaborate with clients cross-functional teams (QA, Production, Engineering, QC) to support validation projects.
Maintain validation documentation and ensure the validated state of equipment and processes.
Draft SOPs.