Qc Supervisor

Agilent Technologies

Colorado, US
Base: $105,280.00 - $164,500.00pyr; bonus/equity: ...
Full time onsite
Cgmp regulated environment experience
Qc personnel supervision skills
Raw material testing oversight
Agilent Technologies is seeking a QC Supervisor in Colorado to oversee Quality Control activities and manage a team of QC analysts in the biopharma sector. The role requires ensuring compliance with regulatory standards and involves hands-on laboratory testing as well as supervisory responsibilities

Job Summary

  • The QC Supervisor will oversee Quality Control activities and supervise a group of analysts to support the development of nucleic acid therapeutics.
  • This role requires ensuring all operations comply with current Good Manufacturing Practices (cGMP) and other regulatory guidance while managing workload priorities.
  • Candidates must be able to write, review, and revise standard operating procedures and assist with deviations and corrective actions.

Matching Summary

Match Score: 85

Agilent Technologies is seeking a QC Supervisor in Colorado to oversee Quality Control activities and manage a team of QC analysts in the biopharma sector. The role requires ensuring compliance with regulatory standards and involves hands-on laboratory testing as well as supervisory responsibilities.

Salary

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

Skills & Requirements

Must-have

  • cGMP regulated environment experience
  • QC personnel supervision skills
  • raw material testing oversight

Nice-to-have

  • Bachelor of Science degree preferred
  • client audit representation experience
  • strategic program development ability

Key Requirements

  • Two years of QC experience required
  • Secondary education with relevant experience
  • Experience leading people or projects

Work Rights

Not specified

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