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QC Chemist

OAKWOOD LABORATORES LLC
Posted 6 days ago, valid for 16 days
Location

Solon, OH 44139, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position is for an entry-level role in Pharmaceutical Quality Control Chemistry located in Solon, OH.
  • Candidates should have a Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field, along with one to two years of hands-on testing experience.
  • The job involves performing analytical testing, documenting activities, executing calculations, and assessing data to ensure material specifications are met.
  • The salary for this full-time position is not specified, but pharmaceutical experience and knowledge of regulatory requirements are advantageous.
  • Ideal candidates will also have experience with instrumentation such as HPLC and GC, and proficiency in Microsoft Suite is required.

Job DetailsJob Location: Solon, OH 44139Position Type: Full TimeJob Category: ScienceWe are adding to our Pharmaceutical Quality Control Chemistry Staff. We are currently seeking entry level individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary. QualificationsWe are seeking individuals with: Bachelor's degree in Chemistry, Biochemistry, Biology, or related field One to two years' experience with hands on testing such as pH, titrations, determination of physical appearance, UV, IR and other wet chemistry tests. Instrumentation work with KF, HPLC, and GC, including instrumentation software a plus. Hands-on analytical chemistry experience Prior success working with regulatory, USP, GLP, GDP, and cGMP requirements. Ability to use Microsoft Suite of tools. Pharmaceutical experience a plus.




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