GMP Validation Specialist: IQ/OQ/PQ, Calibration & Docs

Productlife Group; Lazio; In loco; EUR 34.000 - 39.000; Tempo pieno

Descrizione del lavoro

Productlife Group is seeking a Validation Specialist in Italy (Lazio) to perform calibration and qualification activities for facilities, utilities and equipment, and to prepare validation protocols and reports.

The role requires 3-4 years of experience, a Bachelor’s degree in a relevant field, and fluency in English and Italian. Travel to client sites may be needed along with strong GMP knowledge.

Competenze

• Bachelor's degree in engineering or related life sciences fields.
• 3-4 years of validation experience.
• Professional English and Italian language skills.
• Knowledge of GMP regulations.
• Experience drafting qualification protocols, reports, and SOPs.
• Experience in qualification and commissioning.

Mansioni

• Execute and document calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment.
• Prepare validation protocols, reports and related documentation.
• Maintain validation documentation and ensure the validated state of equipment and processes.
• Collaborate with QA, Production, Engineering, QC on validation projects.
• Draft SOPs and validation master plan.

Conoscenze

English

Italian

Attention to detail

Team working

Problem solving

Interpersonal skills

Willingness to travel

Formazione

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

Strumenti

Office 365

Descrizione del lavoro

Productlife Group is seeking a Validation Specialist in Italy (Lazio) to perform calibration and qualification activities for facilities, utilities and equipment, and to prepare validation protocols and reports.

The role requires 3-4 years of experience, a Bachelor’s degree in a relevant field, and fluency in English and Italian. Travel to client sites may be needed along with strong GMP knowledge.