Validation Officer (CQV)

ProductLife Group; Emilia-Romagna; In loco; EUR 34.000 - 39.000; Tempo pieno

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.

Conoscenze

Problem solving

Interpersonal skills

Writing

Qualification & commissioning

Formazione

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

Strumenti

Office 365

Descrizione del lavoro

Specific activities and responsibilities:

• Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment


• Preparation of validation protocols, reports and related documentation.


• knowledge of GMP regulations


• Ensure compliance with GMP requirements and internal quality standards.


• 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.


• drafting SOPs

Required experience: 3-4 years

Required Education : Bachelor's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related discipline

Required Languages: English + Italian (fully professional/native level)

Required technical skills:

• Office 365 (Word, Excel, PowerPoint, Outlook).


• Experience in qualification and commissioning


• Writing Skills (Sentence Structure and Construction, Clarity and Effectiveness,)


• Experience in drafting qualification protocols, reports, SOPs, and other GMP documentation.


• Good understanding of GMP requirements and validation principles.

Additional experience and/or skills:

• Problem solving


• Good Interpersonal skills


• Flexibility and willingness to travel to client sites as required.

Annual Compensation Range: EUR 34,000 - 39,000

The compensation range indicated in this job posting represents an estimated range for the position. The final remuneration will be determined based on the selected candidate’s experience, skills, qualifications, and internal compensation policies, in accordance with applicable EU and local pay transparency and pay equity requirements.