06 set - Monza
Thermo Fisher Scientific
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
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 our collaborative team as a Equipement Validation Specialist at Thermo Fisher Scientific, where you'll contribute to global healthcare and scientific advancement. In this role, you'll be responsible for ensuring compliance, quality, and operational excellence across our facilities through comprehensive validation activities. Working with advanced technologies and diverse teams,
you'll help maintain high standards in pharmaceutical manufacturing, laboratory operations, and quality control.
REQUIREMENTS:
• Advanced degree with no prior experience required, or Bachelor's degree plus 3-5 years of validation experience in GMP/regulated environment
• Preferred Fields of Study: Engineering, Life Sciences, Chemistry, or related technical field
• Valid driver's license with ability to travel up to 25% as needed
• Comprehensive knowledge of cGMP, FDA regulations, and industry standards (ISO, GAMP5)
• Strong technical writing skills for validation documentation
• Experience with IQ (Installation Qualification) /OQ (Operations Qualification) /PQ (Performance Qualification) protocols and execution is a must
• Minimum 2 years of experience managing validation projects independently is a must
• Consistent record of completing projects on schedule in a deadline-oriented environment is a must
• Proficiency in risk assessment and
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