QC Scientist I - Onsite Cincinnati, OH

Actively Reviewing the Applications

Thermo Fisher Scientific

On-site

Posted 2 weeks ago • Apply by June 16, 2026

Job Description

Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join us at 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 chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients.

Keys to Success

Education:

Bachelor's degree required, no prior experience required
Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field

Experience:

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

Knowledge, Skills, Abilities:

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
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
Ability to work various shifts including nights, weekends, and holidays as needed
Experience in pharmaceutical/regulated environment preferred but not required