QC Scientist I

Thermo Fisher ScientificGreenville, NC
Onsite

About The Position

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.

Requirements

  • Associate’s degree in a science-related field
  • Familiarity with MS Office (Excel, Word, Access)
  • Strong attention to detail and ability to follow standard procedures
  • Critical thinking and problem-solving skills
  • Strong organizational and planning abilities
  • Effective written and verbal communication skills
  • Ability to thrive in a fast-paced, evolving environment
  • 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 screening

Nice To Haves

  • Bachelor’s degree in Biology or related field
  • 2+ years of relevant lab or production-related experience
  • Experience with instrumentation and data reporting
  • Cleanroom or GMP experience
  • Understanding of pharmaceutical GMPs

Responsibilities

  • Perform environmental monitoring using validated methods and procedures
  • Generate, review, and report data in accordance with GMP requirements
  • Compare results to specifications and support investigations (e.g., OOS)
  • Maintain and troubleshoot equipment and instrumentation
  • Review and follow SOPs and analytical procedures
  • Support production timelines and customer needs
  • Ensure adherence to safety, quality, and regulatory standards
  • Complete additional duties as assigned

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

Associate degree

Number of Employees

5,001-10,000 employees

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