Info
High Point, (NC)
High Point, (NC), USA
Regular Full Time
Regular Full Time
Quality Control (QC), Analytical chemist
Quality Control (QC), Analytical chemist

This job offer is no longer active

Contact information is not publicly available anymore.

QC Scientist I

Inactive
Thermo Fisher Scientific - Career

As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.

QC Scientist I

How will you make an impact?

  • QC Scientist I role at Thermo Fisher Scientific Inc. involves maintaining quality and safety standards.

What will you do?

Up to 10% Calibrations/Standardizations/Preparatory Set Up

  • Perform calibrations and standardizations of instruments such as balances and pH meters as required.
  • Standardize volumetric and titrimetric solutions, and prepare buffers and HPLC mobile phases.

Up to 80% Testing/Documentation/Data Review

  • Independently perform complex testing techniques and methods assigned.
  • Conduct testing that requires the highest level of difficulty and precision.
  • Troubleshoot and provide technical assistance with analytical instrumentation like HPLC, GC, FTIR, and UV.
  • Ensure all critical laboratory equipment is calibrated before use.

Up to 5% Housekeeping

  • Maintain and clean laboratory areas, including benches, sinks, and equipment.
  • Occasionally clean laboratory pipettes and other glassware.
  • Dispose of solvents, acids, and other wastes according to company procedures and regulations.

Up to 5% Training and Development

  • Engage in continuous training to improve skills, focusing on technological advancements.
  • Train other analysts in areas of expertise, including chromatographic techniques and laboratory documentation.
  • Actively participate in or lead laboratory projects and propose solutions to encountered problems.

How will you get here?

Education & Experience

  • Bachelor's Degree in Chemistry, Microbiology, Biology, Biochemistry, or a related field, or equivalent experience.
  • Experience in a Quality Control Laboratory in a GMP Pharmaceutical facility is highly desirable.

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, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials
 

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