Validation Associate (CQV)

ProductLife Group; Emilia-Romagna; In loco; EUR 27.000 - 33.000; Tempo pieno

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

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: 1-2 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: up to EUR 30,000

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.