QC Scientist I - Days

Thermo Fisher Scientific•Cincinnati, OH

About The Position

Thermo Fisher Scientific’s Oral Solid Dose (OSD) site in Cincinnati provides drug development and commercial manufacturing services, with expertise in advanced dosage forms. As a QC Scientist I, you will support pharmaceutical manufacturing by testing raw materials, in-process samples, finished products, and stability samples. You will use established analytical methods and laboratory instruments to help ensure product quality while following applicable quality, documentation, and safety requirements. The role is based in a laboratory and cleanroom environment. It may involve strong odors and work with hazardous or toxic materials, and requires adherence to GMP and safety standards and use of required PPE. The position’s stated schedule is standard Monday through Friday, with flexibility to work shifts, including nights, weekends, or holidays, as needed. The company provides competitive wages and an excellent benefits package. Vital work equipment and required PPE are provided.

Requirements

Legally authorized to work in the United States without sponsorship.
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.
Familiarity with analytical methods such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
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 is preferred but not required.
Experience in a pharmaceutical or other regulated environment is preferred.
Experience with microbiological testing, environmental monitoring, or aseptic techniques is an advantage.

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.

Benefits

Medical, dental, and vision benefits effective Day 1.
Paid time off and holidays.
401(k) company match up to 6% after 1 year.
Tuition reimbursement, eligible after 90 days.
Employee referral bonus.
Employee discount program.
Recognition program.
Charitable gift matching.
Company-paid parental leave.
Vital equipment for the role, including computer, monitor, keyboard, and mouse.
Required personal protective equipment, including lab coats, safety glasses, and safety shoes.