QC Scientist I

at  Thermo Fisher Scientific

Florence, South Carolina, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate21 Nov, 2024Not Specified23 Aug, 2024N/AChemistry,Active Pharmaceutical Ingredients,Raw Materials,Latex,Training,BiologyNoNo
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Description:

SUMMARY:

At Thermo Fisher Scientific, we offer a unique opportunity for a QC Scientist I to make a significant impact through their work. As a global leader in serving science with a world-class investment in R&D, we provide a collaborative and inclusive environment where your contributions are valued. Join our fast-growing organization and help us find cures for cancer, protect the environment, ensure food safety, and deliver COVID-19 solutions.

EDUCATION AND EXPERIENCE REQUIREMENTS:

  • Bachelor’s degree in physical science, preferably in Chemistry or Biology
  • Minimum of 0-2 years of experience performing tests or analyses for active pharmaceutical ingredients, raw materials, or microbiological samples
  • Experience with common office software and chromatographic data acquisition systems preferred
  • Equivalent combinations of education, training, and work experience may be considered

PHYSICAL REQUIREMENTS:

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, and organic respirator may be required occasionally

Responsibilities:

  • Perform moderately sophisticated analyses in a laboratory environment following validated procedures and test methods
  • Conduct analytical tests on raw materials, finished products, stability samples, and/or production intermediates
  • Support internal manufacturing and development operations
  • Make detailed observations and communicate test results
  • Assess products for strength, potency, and purity using HPLC, GC, spectroscopy, and wet chemistry techniques
  • Recognize and report out-of-specification or unexpected results
  • Maintain and troubleshoot analytical instrumentation as needed
  • Record and report results of analysis in accordance with Good Documentation Practices
  • Maintain a clean and organized work area, including instrumentation and testing materials
  • Perform all duties in strict compliance with SOP’s, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.
  • Stay current on training modules to contribute to career growth
  • Maintain the needed compliance status required by company and facility standards


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Chemistry or biology

Proficient

1

Florence, SC, USA