• Durham, NC
  • Quick Apply
30+ days ago

Job Description

QC Chemist C will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Will work as a member of the stability team to effectively execute QC analytical testing using established (official and/or in-house) test procedures. This role will entail 80% - 100% of their work being performed at the bench level. The Chemist C will be responsible for review of analytical documents , investigations, maintain the GLP status in lab.

  • Perform assigned in-process, finished product and stability product testing, using various wet chemicals, physical and instrumental techniques ( HPLC, UPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per Finished Product methods.
  • Independently plan and execute testing to meet established time-lines. Perform complicated testing with little supervisory direction.
  • Assist with the preparation or review of Test Procedures, SOPs, Protocols, and CoAs as assigned.
  • Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
  • Perform maintenance and calibrations of laboratory instruments/equipment with little supervisory direction/training.
  • Perform troubleshooting and investigations under the direction of a supervisor.
  • Assist in drafting deviation reports as assigned.
  • Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
  • Review of analytical documents
  • Investigation for OOS/OOT/Deviation and other lab related events
  • Knowledge of EMPOWER Chromatography Data System and LIMS
  • QC experience in Generic Pharmaceutical industries would be preferable
  • Experience in a cGMP environment is required
  • Knowledge and use of Good Documentation practices
  • Knowledge of USP/ICH/FDA guidelines
  • Team player who will assist junior colleagues
  • Willing to work flexible hours to meet product deliverables
  • Ability to learn quickly and have decision making skills that adhere to regulatory practices is required
  • Perform other duties as assigned
  • BS or MS in Chemistry or Pharmaceutical Sciences, or related field
  • Minimum 5+ years of experience in Pharmaceuticals and Analytical testing is desirable
  • Preference shall be given for experience in Inhalation testing on a variety of Inhalation products

Numbers & Facts

LocationDurham, NC

Skills

  • Analysis Skillsunmatched
  • Biotech and Pharmaceuticalunmatched
  • Chemistryunmatched
  • Chromatographic Systemsunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Documentationunmatched
  • FDA (Food and Drug Administration)unmatched
  • GLP (Good Laboratory Practices)unmatched
  • High Performance Liquid Chromatography (HPLC)unmatched
  • ICH Regulationsunmatched
  • IR (Infrared)unmatched
  • Identify Issuesunmatched
  • Laboratory Equipmentunmatched
  • Laboratory Information Management System (LIMS)unmatched
  • Pharmaceutical Analysisunmatched
  • Physical Chemistryunmatched
  • Product Testingunmatched
  • Quality Controlunmatched
  • Regulationsunmatched
  • Reporting Skillsunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Team Playerunmatched
  • Testingunmatched
  • Titrationunmatched
  • UV/VIS (Ultraviolet-Visible Spectroscopy)unmatched

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