Senior Qc Associate, Potency

Genentech

Hillsboro, OR, US
Base: $68,300 to $126,900; bonus/equity: discretio...
Cgmp environment experience
Potency (bioassay) testing expertise
Analytical method development and validation
The QC Specialist supports all activities required of HTO QC, focusing on testing and execution of assignments as assigned by leads, QC specialists, and/or QC management

Job Summary

  • The QC Specialist supports all activities required of HTO QC, focusing on testing and execution of assignments as assigned by leads, QC specialists, and/or QC management.
  • This role serves as the QC department’s subject matter expert in Quality Control Operations processes and provides guidance, mentorship, and training to junior analysts.
  • Relocation benefits are provided and the position offers a discretionary annual bonus based on individual and company performance.

Matching Summary

The QC Specialist supports all activities required of HTO QC, focusing on testing and execution of assignments as assigned by leads, QC specialists, and/or QC management.

Salary

Base: $68,300 to $126,900; Bonus/Equity: discretionary annual bonus; Benefits: detailed benefits package provided

Skills & Requirements

Must-have

  • cGMP environment experience
  • potency (bioassay) testing expertise
  • analytical method development and validation
  • quality control operations processes
  • data interpretation and troubleshooting
  • laboratory equipment maintenance and calibration

Nice-to-have

  • mentorship and training skills
  • cross-functional collaboration
  • continuous improvement initiatives
  • strong communication skills
  • problem-solving capabilities
  • flexibility in work hours

Key Requirements

  • Bachelor’s Degree with 5-7 years cGMP experience
  • 3-5 years experience with Master’s Degree
  • 0-2 years experience with PhD/JD
  • significant potency (bioassay) experience
  • knowledge of GMP regulations
  • experience in analytical/QC testing

Work Rights

Not specified

Tailored Resume

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