QC Scientist I - Days

Thermo Fisher Scientific•Cincinnati, OH

6d•Onsite

About The Position

The QC Scientist I supports pharmaceutical manufacturing at Thermo Fisher Scientific’s Oral Solid Dose site in Cincinnati by testing raw materials, in-process samples, finished products, and stability samples. The role uses established analytical methods and laboratory instruments to help ensure product quality while following quality, documentation, and safety requirements. The site provides drug development and commercial manufacturing services and specializes in advanced dosage forms, including controlled- and sustained-release products, osmotic release dosage forms, liquid-filled hard capsules, controlled substances, and abuse-deterrent technologies. The position is performed in a laboratory and may involve cleanroom conditions, PPE, strong odors, and hazardous or toxic materials.

Requirements

Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, including drug screening.
Bachelor’s degree or equivalent in Chemistry, Biology, Biochemistry, or a related scientific field; equivalent combinations of education, training, and relevant work experience may be considered.
Knowledge of GMP, laboratory documentation, and pharmaceutical quality practices.
Strong attention to detail, problem-solving, and written and verbal communication skills.
Proficiency with Microsoft Office and laboratory information systems.
Ability to work independently and collaboratively.
Ability to stand and walk for extended periods, perform laboratory tasks requiring manual dexterity, and lift up to 50 pounds.
Ability to work in cleanroom environments while wearing required PPE.
Flexibility to work shifts, including nights, weekends, or holidays, as needed.

Nice To Haves

One year of relevant experience; preferred but not required.
Experience in a pharmaceutical or other regulated environment.
Familiarity with analytical methods such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
Experience with microbiological testing, environmental monitoring, or aseptic techniques.

Responsibilities

Perform chemical, physical, and, as assigned, microbiological testing using established procedures.
Test raw materials, in-process samples, finished products, and stability samples.
Use analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods, as applicable.
Support microbiological testing, environmental monitoring, and aseptic practices, as assigned.
Prepare test solutions and maintain laboratory instruments and work areas.
Document work and results accurately in laboratory records and applicable systems.
Identify and communicate unexpected results or testing issues in accordance with procedures.
Follow applicable GMP, SOP, data integrity, and safety requirements.