QC Scientist 1 (Nights 6pm-6am)

Thermo Fisher Scientific•Greenville, NC

About The Position

As part of Thermo Fisher Scientific, the QC Scientist I contributes to global health by performing quality control testing to help ensure the safety and efficacy of pharmaceutical products. The role performs Environmental Monitoring tasks in support of Steriles production within classified areas, including monitoring cleanrooms while sterile products are filled and manufactured. Aseptic technique and knowledge of aseptic gowning are required for work in cleanrooms. The individual is encouraged to follow the company’s 4i Values: integrity, innovation, intensity, and involvement. The typical schedule is 6 p.m. to 6 a.m. on a 2-2-3 rotating schedule. Work takes place in a laboratory and cleanroom environment, with required PPE and adherence to GMP and safety standards.

Requirements

Bachelor’s degree required; no prior experience required.
Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods.
Strong attention to detail and ability to follow standard procedures and maintain data integrity.
Strong problem-solving skills and a logical approach to scientific challenges.
Proficient computer skills, including Microsoft Office and laboratory information systems.
Strong written and verbal communication abilities.
Ability to work independently and collaboratively in a dynamic environment.
Ability to stand and walk for extended periods, lift up to 50 lbs, and perform tasks requiring manual dexterity.
Ability to work in cleanroom environments while wearing required PPE.
Ability to work various shifts, including nights, weekends, and holidays, as needed.

Nice To Haves

Preferred fields of study include Chemistry, Biology, Biochemistry, or a related scientific field.
Experience with microbiological testing, environmental monitoring, and aseptic techniques.
Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards.
Experience in a pharmaceutical or regulated environment is preferred but not required.

Responsibilities

Execute validated environmental test methods for routine environmental monitoring in cleanrooms, including classified areas and aseptic processing.
Recognize and report out-of-specification or unexpected results related to environmental impacts or other causes to support resolution.
Read and verify plates.
Perform daily instrument verifications as required.
Clearly and accurately document testing, analysis, and results.
Record and report analysis results in accordance with prescribed laboratory procedures and systems.
Clean and organize the work area, instrumentation, equipment, and testing materials.
Perform duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, ALCOA, audits, and safety guidelines.
Maintain training and compliance status required by company and facility standards.
Perform other duties as assigned.