QC Scientist I
As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.
QC Scientist I
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Laboratory Setting
Job Description
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.
REQUIREMENTS:
- Bachelor's degree required.
- Preferred Fields of Study: Chemistry, Biology, Biochemistry or 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
- Strong attention to detail with ability to follow standard procedures and maintain data integrity
- Excellent problem-solving skills and logical approach to scientific challenges
- 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
