QC Engineer I - Chemical Analyzers/ Analytical Instruments

Work Schedule

Standard Office Hours (40/wk)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Warehouse

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.

LOCATION: This is a fully onsite position based at our Madison, WI site. 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. 
   

DESCRIPTION:
Be part of our Quality Control team at Thermo Fisher Scientific, where you'll contribute by ensuring the quality and reliability of products that help make the world healthier, cleaner and safer. You'll perform testing and analysis to support the development of innovative therapeutic products. You'll conduct quality control testing of raw materials, in-process samples, and finished products using various analytical techniques. You'll document and analyze test results, participate in investigations, and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.

REQUIREMENTS:

• Bachelor’s degree in engineering, prior experience preferred in quality control in a laboratory environment, manufacturing/biotech industry 
•  Strong knowledge in IS0 requirements, and quality management systems (QMS)
• Strong analytical and problem-solving skills with emphasis in root cause analysis (RCA)
• Lead or support deviation investigations, CAPAs, and change controls
• Ability to follow SOPs, Validation records, Test Reports, batch records and ensuring traceability and compliance
• Support audit readiness (internal, regulatory, customer)
• Strong computer skills in Microsoft Office, and analytical software
•  Excellent attention to detail and organizational skills
•  Ability to work both independently and collaboratively in a cross functional team environment
•  Clear written and verbal communication skills
• Experience with laboratory equipment maintenance and calibration
• Knowledge of relevant regulatory requirements
• Ability to manage multiple priorities effectively
• Flexible scheduling may be required