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Job Details

 

HPLC Method Development Scientist (Full Time)

Location: Concord, Ohio Country: United States of America
 

Essential Responsibilities

  • Develop and validate stability-indicating HPLC procedures for small molecule drug substances and drug products.
  • Perform forced degradation studies and develop stability indicating assay and impurities methods
  • Work in a GMP laboratory. Coordinate the timely and compliant generation of data to support client projects.
  • Perform routine HPLC analysis and validation studies
  • Author protocols and reports. Review data for technical content and regulatory compliance.
  • Maintain current expertise with relevant ICH, GMP, and FDA guidelines.

Requirements Educational Qualifications

B.S. to Ph.D. in chemistry or related field with 5+ years analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good manufacturing practices (GMP) laboratory is required.

Specific Skills and Requirements

  • Experience in standard lab instrumentation (HPLC, UPLC, etc.)
  • Experience with LCMS or GC preferred but not required
  • Be proficient in LIMS, Microsoft Excel, and Word
  • Must have basic knowledge chemicals their properties, structure, reactivity, and be able to handle with safe and appropriate techniques.
  • Must have basic knowledge of arithmetic, algebra, and statistics.
  • Must be able to communicate effectively with all plant and office personnel.
  • Must be able to effectively multi-task

Posted Date: 17 Jul 2018 Reference: CB Company: OlonRicerca Bioscience Contact: Human Resources