Qc Supervisor

Agilent Technologies

Colorado, US
Base: $105,280.00 - $164,500.00pyr; bonus/equity: ...
Full time (onsite)
Supervise qc personnel and analysts
Ensure cgmp regulatory compliance
Review analytical data and protocols
Agilent Technologies is seeking a QC Supervisor to oversee Quality Control activities in their Colorado operations, focusing on nucleic acid therapeutics. The role involves supervising QC analysts, ensuring compliance with regulatory standards, and participating in laboratory testing and audits

Job Summary

  • The role involves overseeing Quality Control operations to ensure compliance with current Good Manufacturing Practices (cGMP) while supporting the development of nucleic acid therapeutics.
  • The supervisor is responsible for managing staff workload, reviewing analytical data, and leading corrective actions during client audits and regulatory inspections.
  • This position offers a competitive salary range of $105,280.00 - $164,500.00 per year plus eligibility for bonus, stock, and benefits.

Matching Summary

Match Score: 85

Agilent Technologies is seeking a QC Supervisor to oversee Quality Control activities in their Colorado operations, focusing on nucleic acid therapeutics. The role involves supervising QC analysts, ensuring compliance with regulatory standards, and participating in laboratory testing and audits.

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 protocols
  • Manage raw material testing schedules
  • Lead CAPA investigations and audits

Nice-to-have

  • Experience with nucleic acid therapeutics
  • Customer-centered culture mindset
  • Strategic program implementation skills
  • Industry association representation experience

Key Requirements

  • Secondary education with relevant experience
  • Two years of QC experience required
  • Two years experience leading people or projects
  • Experience in cGMP regulated environment
  • Ability to write and review protocols

Work Rights

Not specified

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