Quality Validation Specialist

TN Italy; Lazio; In loco; EUR 40.000 - 55.000; Tempo pieno

Descrizione del lavoro

A leading company in drug containment solutions is seeking a Quality Validation Specialist in Cisterna di Latina. The role involves managing validation processes, ensuring compliance with quality standards, and participating in audits. Ideal candidates will have a scientific master's degree and relevant experience in validation within the pharmaceutical or medical device sectors.

Competenze

• At least 2 years’ experience in validation within a multinational, preferably in pharmaceuticals or medical devices.

Mansioni

• Executing qualification and validation activities to meet targets.
• Contributing to the development and implementation of validation practices.
• Preparing reports to monitor validation KPIs.

Conoscenze

Knowledge of internal audit processes

Proficiency with relevant IT tools

Formazione

Scientific Master’s Degree

Descrizione del lavoro

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Quality Validation Specialist, Province of Latina

Client:

Location: Province of Latina, Italy

Job Category: Other

EU work permit required: Yes

Job Reference: bb282dfb915b

Job Views: 3

Posted: 15.05.2025

Expiry Date: 29.06.2025

Job Description:

Job Description

We are looking for a Validation Specialist to join the Quality Validation team based in Cisterna di Latina (LT).

Stevanato Group is an Italian multinational manufacturing company. We develop and produce drug containment solutions in glass and plastics.

The main production process involves the processing of glass tubes by forming and subsequent cleaning and sterilization of the containers using highly automated machinery.

The Validation team is responsible for ensuring the approval and validation of all production processes, supporting IT systems, utilities, test methods, equipment, and cleaning processes, producing products that meet internal and regulatory standards. The team operates across multiple sites.

The main activities include:

1. Validation Management: Executing qualification and validation activities to meet targets, supporting validation planning, and providing validation documentation.
2. Guidelines and Procedures: Contributing to the development and implementation of validation practices and ensuring compliance with quality management systems.
3. Quality Audit Management: Participating in audits and customer meetings, providing technical support, and implementing corrective actions.
4. Reporting and Monitoring: Preparing reports to monitor validation KPIs, identifying deviations, and proposing corrective actions.

Qualifications:

• Scientific Master’s Degree
• At least 2 years’ experience in validation within a multinational, preferably in pharmaceuticals or medical devices
• Knowledge of internal audit processes, applicable regulations, standards, and global manufacturing practices
• Proficiency with relevant IT tools

Availability to travel within the country is required.