Hybrid GMP Validation Specialist – IQ/OQ/PQ Expert

ProductLife Group; Parma; Ibrido; EUR 45.000 - 65.000; Tempo pieno

Descrizione del lavoro

ProductLife Group is seeking an experienced Validation Specialist Officer to join its Center of Expertise Engineering, based near Parma, Italy, with a hybrid working policy. You will own qualification and validation activities (IQ/OQ/PQ) for facilities, utilities and equipment, ensuring GMP compliance and high-quality documentation, and collaborating with QA, Production and Engineering teams on validation projects.

Travel to client sites may be required.

Competenze

• Bachelor's/Master's degree in Engineering or Life Sciences.
• 3+ years of GMP-regulated validation experience.
• Experience with IQ/OQ/PQ qualification and commissioning.
• Strong technical writing and GMP documentation skills.
• Proficiency in MS Office 365.

Mansioni

• Plan, execute, and document IQ/OQ/PQ for facilities, utilities and equipment.
• Prepare and review validation protocols and reports.
• Coordinate qualification activities and ensure timely documentation.
• Ensure GMP compliance and support CAPAs and risk assessments.

Conoscenze

GMP knowledge

Validation documentation

IQ/OQ/PQ experience

Technical writing

MS Office 365

Formazione

Bachelor's or Master's in Engineering or Life Sciences

Strumenti

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Descrizione del lavoro

ProductLife Group is seeking an experienced Validation Specialist Officer to join its Center of Expertise Engineering, based near Parma, Italy, with a hybrid working policy. You will own qualification and validation activities (IQ/OQ/PQ) for facilities, utilities and equipment, ensuring GMP compliance and high-quality documentation, and collaborating with QA, Production and Engineering teams on validation projects.

Travel to client sites may be required.