Qc Supervisor - Second Shift

Agilent Technologies

Colorado, US
Base: $105,280.00 - $164,500.00pyr; bonus/equity: ...
Second shift (2:30 pm - 11 pm)
Supervise qc personnel and analysts
Ensure cgmp regulatory compliance
Review analytical data and methods
Agilent Technologies is seeking a QC Supervisor for their second shift in Colorado, responsible for overseeing Quality Control activities and ensuring compliance with Good Manufacturing Practices. The ideal candidate will have QC experience and supervisory skills, working within a team dedicated to the development of nucleic acid therapeutics

Job Summary

  • The role involves overseeing Quality Control activities and supervising a team of analysts to support the development of nucleic acid therapeutics.
  • Candidates must ensure all operations comply with current Good Manufacturing Practices (cGMP) and assist with regulatory inspections and audits.
  • The position offers a competitive salary range of $105,280.00 to $164,500.00 per year plus eligibility for bonus, stock, and benefits.

Matching Summary

Match Score: 85

Agilent Technologies is seeking a QC Supervisor for their second shift in Colorado, responsible for overseeing Quality Control activities and ensuring compliance with Good Manufacturing Practices. The ideal candidate will have QC experience and supervisory skills, working within a team dedicated to the development of nucleic acid therapeutics.

Salary

Base: $105,280.00 - $164,500.00/yr; Bonus/Equity: Eligible for bonus and stock; Benefits: Eligible for benefits

Skills & Requirements

Must-have

  • Supervise QC personnel and analysts
  • Ensure cGMP regulatory compliance
  • Review analytical data and methods
  • Manage in-process testing timelines
  • Lead CAPA investigations and audits

Nice-to-have

  • Experience leading people formally or informally
  • Customer-centered culture mindset
  • Ability to translate regulations into plans
  • Industry association representation experience

Key Requirements

  • Secondary education with relevant experience
  • Two years of QC experience
  • Experience in a cGMP environment preferred
  • One year of leadership experience preferred

Work Rights

Not specified

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