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Job Details


Scientist, QC (Full Time)

Location: Concord Ohio Country: United States of America

Essential Responsibilities

  • Perform routine HPLC analysis in a QC pharmaceutical laboratory
  • Coordinate raw material testing in a materials management system
  • Conduct inspections of manufacturing supplies
  • Experience with sampling raw materials and intermediates
  • Experience with chromatography support for equipment cleaning
  • Coordinate the timely and compliant generation of data to support client projects
  • Review data for technical content and good record keeping practices
  • May also perform GC analysis

Requirements Educational Qualifications

B.S. to Ph.D. in chemistry with 3+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control, and interaction with quality assurance is required.

Specific Skills and Requirements

Experience in standard lab instruments (HPLC, analytical balances, pH meter, etc.)

Be proficient in Microsoft Excel and Word

Must have basic chemical knowledge and be able to handle materials safely.

Posted Date: 14 Oct 2019 Reference: CB Company: OlonRicerca Bioscience Contact: Bernadette Armbruster