TitleQC Analyst I/II- Temporary
Department NameQuality Control
 The purpose of this position is to carry out the Worksheet Validation Project. The project duration is 6 months.  

Responsibilities (Including but not limited to):
  • Assist in write-up and review of Worksheet Validation Protocols.
  • Execute Worksheet Validation Protocols.
  • Assist in completing deviations related to the Worksheet Validation
  • Maintain organized records and comply with GMP documentation practices.
  • Assist in completing reports related to Worksheet Validation.
  • 1 year of relevant hands-on pharmaceutical laboratory experience.
  • BS degree in Chemistry from an accredited college or university or equivalent experience.
  • Demonstrated computer proficiency, e.g., word processing, spreadsheets, graphing, etc.. Proficiency in MS Excel is preferred.
  • Good knowledge of cGMPs and laboratory practices.
  • Familiar with basic laboratory instruments.
  • Excellent observation skills and problem solving abilities.
  • Ability to follow analytical procedures and protocols.
  • Good laboratory techniques.
  • Ability to work in a methodical and organized fashion.
  • Ability to write in a concise, logical fashion.
  • Ability to manage multiple responsibilities with a high degree of self motivation.
  • Good oral, written, and interpersonal English communication skills.
  • Ability to effectively utilize scientific information resources within the assigned area of responsibility.