QC Scientist 1 (Nights 6pm-6am)

Thermo Fisher Scientific

Greenville, NCFresher1h agovia LinkedIn

This job at a glance

Who can apply
New grads, no experience needed · Bachelor's degree
Must know
AuditingMicrosoft Office
Work
On-site in Greenville
Pay
Not stated by the employer.
Skill demand
Auditing27%Microsoft Office24%of 99 similar entry-level jobs posted in the US this week
Listed
Oct 31, 2026 · still open

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About the Role

Join Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the 4i Values: integrity, innovation, intensity, and involvement. The job function includes aseptic technique, requiring knowledge of aseptic gowning and working in cleanrooms to monitor the area during sterile product filling and manufacturing.

Typical shift hours are 6pm-6am on a 2-2-3 rotating schedule.

Key Responsibilities

  • Execute validated environmental test methods for routine environmental monitoring in clean rooms (i.e., classified areas and aseptic processing).
  • Recognize and report out-of-specification or unexpected results due to environmental impacts or other to reach resolution.
  • Reading and verification of plates.
  • Perform daily instrument verifications as required.
  • Clearly and accurately communicate the results of work by creating documentation of the testing/analysis and obtained results.
  • Record and report results of analysis in accordance with prescribed lab procedures and systems.
  • Cleans and organizes work area, instrumentation/equipment, and testing materials.
  • Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), ALCOA, Audits, and Safety guidelines.
  • Maintain the necessary training and compliance status required by company and facility standards.
  • And other duties as assigned.

Requirements & Tech Stack

  • Bachelor's degree required.
  • Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods.
  • Experience with microbiological testing, environmental monitoring, and aseptic techniques.
  • Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards.
  • Strong attention to detail with ability to follow standard procedures and maintain data integrity.
  • Excellent problem-solving skills and logical approach to scientific challenges.
  • Proficient computer skills including Microsoft Office and laboratory information systems.
  • Strong written and verbal communication abilities.
  • Ability to work both independently and collaboratively in a dynamic environment.
  • Ability to work various shifts including nights, weekends, and holidays as needed.
  • Experience in pharmaceutical/regulated environment preferred but not required.

Qualifications

  • Bachelor's degree required, no prior experience required.
  • Preferred Fields of Study: Chemistry, Biology, Biochemistry, or related scientific field.
  • Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity.
  • Must be able to work in cleanroom environments wearing required PPE (Personal Protective Equipment).

Environmental Conditions

  • Able to lift 40 lbs. without assistance.
  • Adherence to all Good Manufacturing Practices (GMP) Safety Standards.
  • Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed.
  • Laboratory Setting.
  • Loud Noises (Equipment/Machinery).
  • Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.).
  • Standing for full shift.
  • Strong Odors (chemical, lubricants, biological products etc.).

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