Scientist - Analytical

Olon Ricerca BioscienceConcord, OH
310d

About The Position

The Analytical Scientist position involves performing HPLC-MS/MS (QQQ and QTOF) and NMR method development and validation to support drug development. The role includes conducting method development, structural characterization, impurity isolation and identification, and quantitative analysis. The scientist will perform routine HPLC, HPLC-MS/MS, GCMS, and NMR analysis, coordinate the timely and compliant generation of data to support client projects, and participate in ongoing equipment maintenance and qualification. Additionally, the scientist will review data for technical content and regulatory compliance, interact with clients to design scientifically sound studies, and maintain current expertise with all appropriate ICH, GMP, and FDA guidelines.

Requirements

  • B.S. to Ph.D. in chemistry or related field with 2+ years analytical laboratory experience or equivalent combination of education and experience is required
  • Relevant experience with good manufacturing practices (GMP) is desired
  • Experience with HPLC, HPLC-MS/MS, NMR, semi-prep chromatography, lyophilization, etc.
  • Experience with isolation and identification of impurities
  • Experience with GC-MS, FTIR, desirable, but not required
  • Experience with lab procedures (extraction, solid phase extraction, dilution, etc.)
  • Proficient in Microsoft Excel, Word, and PowerPoint
  • Basic knowledge of chemicals, their properties, structure, reactivity, and safe handling techniques
  • Effective communication skills with coworkers and good writing skills
  • Ability to effectively multitask

Nice To Haves

  • Experience with GC-MS and FTIR

Responsibilities

  • Perform HPLC-MS/MS (QQQ and QTOF) and NMR method development and validation supporting drug development
  • Conduct method development, structural characterization, impurity isolation and identification, and quantitative analysis
  • Perform routine HPLC, HPLC-MS/MS, GCMS, and NMR analysis
  • Coordinate the timely and compliant generation of data to support client projects
  • Participate in ongoing equipment maintenance and qualification
  • Review data for technical content and regulatory compliance
  • Interact with clients to design scientifically sound studies
  • Maintain current expertise with all appropriate ICH, GMP, and FDA guidelines

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What This Job Offers

Job Type

Full-time

Industry

Chemical Manufacturing

Education Level

Bachelor's degree

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