QC Scientist I

Discover impactful work:

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.

Shift Schedule: 12hr day shift position. 7 AM - 7 PM

2 days on, 2 days off and every other weekend, 12hr shift

Day in the Life:

Conduct day-to-day testing activities including chemical, physical, and microbiological analyses of raw materials, in-process samples, finished products, and stability samples

Complete accurate documentation and reporting duties in compliance with GMP standards and regulatory requirements

Collaborate with other departments including Manufacturing, Quality Assurance, and Research & Development to support production goals and quality objectives

Perform equipment maintenance and calibration tasks to ensure analytical instruments remain in proper working condition

Participate in investigation and troubleshooting activities to identify root causes of out-of-specification results or testing anomalies

Support training responsibilities including onboarding new team members and sharing technical expertise with colleagues

Keys to Success:

Bachelor's degree required, no prior experience 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