QC Scientist I

Thermo Fisher ScientificSaint Louis, MO
1hOnsite

About The Position

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 and physical 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. The job is very fast paced and changing therefore the ability to switch tasks quickly is desired. In the department, we perform inspections and/or sampling on incoming materials including bulk gasses and cell banks. This includes the review and disposition of raw materials. You will support general sampling functions such as ordering and stocking sampling supplies, maintaining chemical retain inventory, and managing hazardous waste disposal. You will assist with drafting and revising standard operating procedures (SOP's) and other department owned documentation. You will draft or assist in deviation investigations to ensure timely closure of investigations. Lastly, assist in completing preventative maintenance tasks for the department.

Requirements

  • Bachelor's degree preferred, High School Degree or equivalent required with 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

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 chemical and physical analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP).
  • Conduct testing of raw materials, in-process samples, finished products, and stability samples.
  • Perform inspections and/or sampling on incoming materials including bulk gasses and cell banks.
  • Review and disposition of raw materials.
  • Support general sampling functions such as ordering and stocking sampling supplies, maintaining chemical retain inventory, and managing hazardous waste disposal.
  • Assist with drafting and revising standard operating procedures (SOP's) and other department owned documentation.
  • Draft or assist in deviation investigations to ensure timely closure of investigations.
  • Assist in completing preventative maintenance tasks for the department.
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