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Engineer II, QC

Job

Thermo Fisher Scientific

Madison, WI (In Person)

Full-Time

Posted 2 weeks ago (Updated 5 days ago) • Actively hiring

Expires 6/3/2026

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Job Description

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards 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 Quality Control team at Thermo Fisher Scientific where you'll make meaningful contributions to our mission of enabling customers to make the world healthier, cleaner and safer. As an Engineer/Scientist II, QC, your work will center on strengthening quality frameworks and enabling proactive, data-based decision-making. You'll collaborate cross-functionally to analyze data, identify trends and sources of variability, and implement control strategies to enhance product quality in an analytical instrumentation manufacturing environment. This role offers excellent opportunities for professional growth while working alongside colleagues who share your commitment to science and quality.
REQUIREMENTS
Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of experience, preferably in a research or manufacturing environment
Preferred Fields of Study:
Science or Engineering Additional certifications in Quality Control/GMP practices beneficial Understanding of analytical techniques such as spectroscopy preferred Experience in data analysis and investigation of out-of-specification results Strong documentation skills and proficiency with information management systems Knowledge of relevant regulatory standards (ISO, FDA, USP, EP) preferred Excellent attention to detail and ability to follow written/verbal procedures accurately Strong organizational and time management skills Ability to work both independently and collaboratively in a team environment Proficiency in Microsoft Office applications Clear written and verbal communication skills in English Knowledge of Lean/Six Sigma principles beneficial

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