Di/qc & Admin Lead

Johnson & Johnson Innovative Medicine

Santa Clara, California, United States of America
Base: $150,000 - $170,000; bonus/equity: not speci...
Hybrid
21 cfr part 58 compliance
Glp program support
Data integrity review
Support execution of preclinical studies for robotic and digital solutions for regulatory approval and clinical acceptance

Job Summary

  • Support execution of preclinical studies for robotic and digital solutions for regulatory approval and clinical acceptance.
  • Implement Quality Control processes and procedures to optimize quality control function in support of compliance under 21 CFR 58.
  • Oversee archive including electronic, physical, wet tissues, test article retains, and test articles dispensary.

Matching Summary

Support execution of preclinical studies for robotic and digital solutions for regulatory approval and clinical acceptance.

Salary

Base: $150,000 - $170,000; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • 21 CFR Part 58 compliance
  • GLP program support
  • Data integrity review
  • Equipment maintenance and calibration
  • Internal system inspections

Nice-to-have

  • Process improvement leadership
  • Cross-functional team collaboration
  • Subject Matter Expert on GLP

Key Requirements

  • Master's degree in Biotechnology or related field
  • 2 years of experience in DI/QC & Admin Lead-related occupation

Work Rights

Not specified

Tailored Resume

Cover Letter