QC Scientist I

Thermo Fisher Scientific•Saint Louis, MO

About The Position

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. We have 3 positions available.

Requirements

Bachelor's degree required, no prior experience required
Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods
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
Must be legally authorized to work in the United States now or in the future, without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening

Nice To Haves

Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field
Experience with microbiological testing, environmental monitoring, and aseptic techniques
Experience in pharmaceutical/regulated environment preferred but not required

Responsibilities

Perform testing on In-Process, DS release, DP release, DS stability, DP Stability, and various other non-routine samples, ensuring timely delivery for projects
Conduct GMP testing in an analytical laboratory environment using Separation Techniques, BioAssay Analysis and Compendia test methods (i.e.,Reverse Phase, SEC, Titer concentration, iCE, pH, Osmolarity, Residual DNA, Appearance)
Compiles data for documentation of test procedures, prepares reports.
Collaborate with team members and other departments such as quality assurance and data reviewers.
Contributes to the development of new concepts, techniques, and standards.
Recognize and report invalid/ lab incident/ out-of-specification/ out-of-trend results to laboratory management; recommend solutions.
Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines.
Participate in laboratory activities, performing safety inspections and ordering supplies.