Engineer II, QC

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

LOCATION:

This is a fully onsite position based in Madison, WI. Unfortunately, relocation assistance is NOT provided.

* Must be legally authorized to work in the United States without sponsorship now or in the future.

* Must be able to pass a comprehensive background check, which includes a drug screen.

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, Bachelor's Degree with 2 years of experience, preferably in a research or manufacturing environment

* Equivalent experience (4 years plus) will also be considered in lieu of a degree. HS diploma / GED is required

* 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