Di/qc & Admin Lead

Johnson & Johnson

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

Job Summary

  • Support execution of preclinical studies required to competitively position robotic and digital solutions for regulatory approval and clinical acceptance.
  • Implement Quality Control processes and procedures spanning from implementing quality standards through developing internal processes to optimize the quality control function in support of compliance under 21 CFR 58.
  • Responsible for resourcing of lab activities and facility utilization, including managing purchase orders, vendors, inventory tracking, and specimens and supplies orders.

Matching Summary

Support execution of preclinical studies required to competitively position 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 laboratory compliance
  • GLP program oversight
  • 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 or equivalent
  • 2 years of related experience

Work Rights

Not specified

Tailored Resume

Cover Letter