Thermo Fisher

QC Scientist I

St. Louis, Missouri, USA Full time

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

How will you make an impact:
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.

A Day in the Life:

  • 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. 


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

Excellent Benefits

OTHER

  • Relocation assistance is NOT provided
  • 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