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Equipment Validation Compliance Specialist

Pubblicato il 23-09-2026 - Thermo Fisher Scientific in Monza

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION
Join us as a Equipment Validation Compliance Specialist at Thermo Fisher Scientific, where you'll contribute to ensuring product quality and regulatory compliance. In this position, you'll be responsible for reviewing and approving qualification protocols, qualification reports and technical documentation related to equipment and systems requiring qualification,



ensuring compliance with applicable regulatory requirements and company procedure. Working with cross-functional teams, you'll help maintain our high standards of quality while supporting continuous improvement initiatives. This role offers excellent opportunities for professional growth within an established leader in serving science.

KEY RESPONSIBILITIES
• Review technical documentation related to equipment and systems requiring qualification, ensuring compliance with current regulatory requirements (cGMP, FDA, and other applicable regulations) and internal procedures.
• Review and approve qualification protocols and reports (IQ/OQ/PQ), ensuring their accuracy, completeness, and compliance with applicable GMP regulations and company standards.
• Support equipment qualification activities by providing quality oversight and evaluating technical issues to ensure proper execution of IQ/OQ/PQ p

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