As a QC Scientist I at Thermo Fisher Scientific, you will be part of a global team dedicated to making the world healthier, cleaner, and safer. The Greenville, NC site is a large pharmaceutical manufacturing and packaging campus specializing in solid oral dose and sterile manufacturing, including aseptic filling, biologics production, lyophilization, and advanced drug product technologies. This role is crucial for performing environmental monitoring activities to support sterile manufacturing within classified cleanroom environments. You will ensure product quality, maintain compliance with Good Manufacturing Practices (GMP) standards, and contribute to the production of critical pharmaceutical products. The position operates in a fast-paced, team-oriented environment, embodying Thermo Fisher’s 4i Values: Integrity, Innovation, Intensity, and Involvement. Daily tasks include reviewing schedules, performing environmental monitoring in cleanrooms, conducting routine and batch-related testing using validated methods and instrumentation, gowning for extended periods, analyzing samples, verifying results, documenting data, supporting production lines, collaborating with team leads for training, and assisting with troubleshooting and continuous improvement initiatives. Most work is performed directly in cleanroom environments supporting production.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees