Equipment Validation Specialist
Pubblicato il 05-08-2026 - Thermo Fisher Scientific in Ferentino
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office 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 Specialist at Thermo Fisher Scientific, where you'll contribute to ensuring product quality and regulatory compliance. You'll be responsible for planning, executing, and documenting validation activities across equipment, processes, and computer systems. 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. **REQUIREMENTS**:
- Bachelor's Degree required. Preferred Fields of Study: Engineering, Chemistry, Biotechnology, Biology, or related scientific field.
- Strong knowledge of validation principles including IQ/OQ/PQ protocols and FDA/EMA regulatory requirements.
- Proficient in statistical analysis and use of tools like Minitab.
- Experience with equipment qualification, process validation, and cleaning validation.
- Strong documentation skills and attention to detail.
- Expertise in Microsoft Office suite and validation management systems.
- Excellent written and verbal communication skills in English.
- Ability to work independently and as part of cross-functional teams.
- Strong problem-solving abilities and analytical mindset.
- Experience with risk assessment methodologies.
- Knowledge of data integrity requirements and 21 CFR Part 11 compliance.
- Ability to manage multiple priorities effectively.
- Travel between sites may be required.
- Flexible schedule may be necessary for time-sensitive validation activities.