GMP Validation Associate & Documentation Specialist

ProductLife Group

Emilia-Romagna

In loco

EUR 27.000 - 33.000

Tempo pieno

43 ore fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

ProductLife Group is seeking a Validation Specialist with 1-2 years of experience to execute calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment. The role includes drafting validation documentation and SOPs, ensuring GMP compliance.

The candidate will collaborate with QA, Production, Engineering and QC teams, maintain validated states of equipment and processes, and be comfortable traveling to client sites. Proficiency in English and Italian required.

Competenze

  • 1–2 years of experience in validation, qualification and commissioning.
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, Pharmacy or related field.
  • Proficient in English and Italian at professional/native level.

Mansioni

  • Execute and document calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment.
  • Prepare validation protocols, reports and related documents.
  • Ensure compliance with GMP regulations and internal quality standards.
  • Support change controls, deviations, CAPAs, and risk assessments related to validation.
  • Collaborate with client cross-functional teams (QA, Production, Engineering, QC) on validation projects.
  • Maintain validation documentation and ensure equipment/processes stay validated.
  • Draft SOPs.
  • Travel to client sites as required.

Conoscenze

Office 365
Qualification & commissioning
Writing skills
Qualification protocols
GMP knowledge

Formazione

Bachelor's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or related field

Descrizione del lavoro

ProductLife Group is seeking a Validation Specialist with 1-2 years of experience to execute calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment. The role includes drafting validation documentation and SOPs, ensuring GMP compliance.

The candidate will collaborate with QA, Production, Engineering and QC teams, maintain validated states of equipment and processes, and be comfortable traveling to client sites. Proficiency in English and Italian required.

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