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 through quality control testing that helps 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. The work requires aseptic technique, knowledge of aseptic gowning, and adherence to the company’s values of integrity, innovation, intensity, and involvement. The typical schedule is 6 p.m. to 6 a.m. on a rotating 2-2-3 schedule. The role is performed in a laboratory and cleanroom setting, with exposure to loud equipment or machinery and strong odors from chemicals, lubricants, or biological products. Required conditions include wearing PPE and following GMP safety standards and cleanroom restrictions on personal products and adornments.

Requirements

Bachelor’s degree required; no prior experience required.
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.
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.
Experience in a pharmaceutical or regulated environment; preferred but not required.

Responsibilities

Execute validated environmental test methods for routine environmental monitoring in cleanrooms, classified areas, and aseptic processing environments.
Recognize and report out-of-specification or unexpected results related to environmental impacts or other causes, and help reach resolution.
Read and verify plates.
Perform daily instrument verifications as required.
Clearly and accurately document testing, analysis, and results.
Record and report analytical 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, GMP, GLP, ALCOA, audit, and safety guidelines.
Maintain required training and compliance status under company and facility standards.
Perform other duties as assigned.