Quality Control Analyst

4 weeks ago

washington, United States Endeavor Consulting Group, LLC Full time

Leading Global OTC / Global Personal Care corporation has an immediate need for a QC Chemist / Analytical Scientist, at the world headquarters located in the Fort Washington, PA area. This is an excellent opportunity to join one of the world’s most respected and trusted companies.

MINIMUM QUALIFICATIONS

  • BS degree in Chemistry or related disciplines
  • Experience in the OTC / Personal Care or associated GMP industry
  • Perform analysis utilizing analytical instruments, notably chromatographic instruments and perform instrumental and wet chemistry testing using HPLC, UPLC, GC, FT-IR, UV/VIS, LC-MS, dissolution apparatus, Karl Fisher titration, and wet chemistry as required.
  • Experience with QC analysis to include: HPLC, Water, Mass Spec, FTIR, UV, GC,
  • Perform Assay Testing
  • Test Method development and Validation
  • Ability to effectively organize, multitasks, and works in a fast-paced, deadline driven work environment.
  • Excellent written and oral communications skills (technical writing a plus)
  • Ability to communicate in a proactive and solutions-focused manner, including keeping management aware of potential issues.
  • Exhibit professional interpersonal skills.
  • Communicate effectively and ability to work in a team environment.
  • Exhibit detail oriented documentation skills.
  • Basic computer knowledge, including Microsoft word and excel (used daily).

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

  • Perform QC analysis to include: HPLC, Water, Mass Spec, UV, GC, melting point, Optical Rotation, TLC and misc. wet chemistry lab work and other related analytical equipment used for control quality of the GMP facility and other related analytical equipment used for control quality of the GMP facility. This work may include calibration and validation of these methods
  • Control raw material used in the manufacturing facility for GMP to include receiving, quarantine, testing and QC release
  • Investigate any deviation or out of specification as necessary related to QC work performed as instructed by supervisor
  • Support validation, stability and material management as necessary to include but not limited to analytical work, documentation and quality GMP procedures

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