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Associate Scientist I - R&D

MyKelly
High Point, North Carolina, United States
$22-$26 an hour
Full-time

Job Description : High Point, NC

Shift : Days, 8am-5pm

Pay Rate : $22-$26

How will you make an impact?

The Associate Scientist is responsible for the complete testing and results documentation of any finished goods, stability and in-process samples within the QC Chemistry Laboratory, in a manner consistent with established standards.

What will you do?

  • Up to 50% Calibrations / Standardizations / Preparatory Set Up
  • Perform calibrations / standardizations of instruments such as balances and pH meters
  • Perform standardizations of volumetric / titrimetric solutions, and prepares buffers and HPLC mobile phase, among other solutions.
  • Prepare and stage the solution for testing by senior analysts
  • Understand and follow the Data integrity Up to 20% Testing / Documentation / Data Review
  • Independently perform core techniques or methods as assigned for testing on raw materials and in-process samples.
  • Perform testing that has the highest level of difficulty compared to other testing methods.
  • Demonstrate ability to troubleshoot and provide technical assistance to other analysts in the area of analytical instrumentation such as HPLC, GC, FTIR, and UV.
  • Ensure that the calibration of critical laboratory equipment is current before use. Up to 25% Housekeeping
  • Clean and organize all laboratory areas including bench, sinks, drawers, cabinets, solvent cabinets, fume hoods, refrigerators, freezers, desiccators and storage areas.
  • Occasionally clean laboratory pipettes and other glassware.
  • Maintain laboratory instruments disposing of wastes, cleaning them and replacing consumable parts as required.
  • Ensure the lab areas are audit ready at all times Up to 5% Training and Development
  • Participate in ongoing training for the development of skills and responsibility with an emphasis on technology.
  • Perform training of other analysts in areas of expertise, such as but not limited to chromatographic techniques, laboratory documentation, and documentation review.
  • Ability to actively participate on various and / or lead laboratory projects or teams and propose solutions to problems encountered by such teams. Education & Experience
  • Bachelor's Degree in Chemistry, Microbiology, Biology, Biochemistry or related field, Experience in a Quality Control Laboratory in GMP Pharmaceutical facility preferred.

9377855

2 days ago
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