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Quality Control Analyst I/II

Job Description:

The Quality Control Analyst I/II will work in the Quality Control Laboratory to support the routine incoming raw materials and product release testing activities.  To support all activities to assure that all products are defect free and cGMP compliant with technical specifications.

  • Responsible for physical and chemical evaluation of final product, intermediate/in-process products, raw materials, and container closures/packaging
  • Duties include performing method validations, establishing specifications, creating Standard Operating Procedures, creating validation protocols

Requirement:

  • Has knowledge of commonly-used laboratory instruments like HPLC, GC, FT-IR, UV-Vis and Dissolution Testers
  • Familiar with cGMP, FDA regulations
  • Bachelor’s Degree in Science, preferably Chemistry, or an associated field of study
  • Excellent problem solving and interpersonal communication skills.
  • Ability to handle multiple tasks concurrently, and in a timely fashion.
  • Computer literate.
  • Must be detail-oriented, conscientious and have high reading comprehension skills.
  • Must have basic understanding of laboratory instrumentation.
  • Must be capable of performing basic laboratory techniques like weighing, pipetting and solution dilution.
  • Must be able to communicate effectively with supervisors and peers.
  • Must be able to consistently demonstrate self-motivation and the ability to think independently.
  • May be required to work flexible hours and overtime on short notice.
  • Physical Demands
  • Must be able to occasionally lift and carry items weighing up to approximately 25 lbs.
  • Must be able to walk around facility, regularly required to sit, stand, walk, reach with arms

Required Education:

Bachelor's

Required Experience:

2-4 years GMP experience in pharmaceutical manufacturing facility

 

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