Investigator - Lenti

J&J FAMILY OF COMPANIES

Raritan, New Jersey, United States
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
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Root cause analysis investigations
Regulatory compliance assurance
Quality nonconformance reporting
** Johnson & Johnson is seeking an Investigator for their Lenti unit in Raritan, NJ, who will lead investigations into nonconformances and recommend corrective measures to ensure compliance with quality standards. The ideal candidate will possess a Bachelor’s degree in Engineering or Life Sciences and have at least two years of relevant experience in the biopharmaceutical or pharmaceutical industries. **

Job Summary

  • The Investigator will lead cross-functional investigations teams to identify true root cause of investigations, conduct risk assessments, and assess the impact of nonconformances.
  • They will recommend and coordinate implementation for corrective/preventative measures to improve compliance and ensure consistent quality standards are maintained.
  • Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects diversity and dignity of employees.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an Investigator for their Lenti unit in Raritan, NJ, who will lead investigations into nonconformances and recommend corrective measures to ensure compliance with quality standards. The ideal candidate will possess a Bachelor’s degree in Engineering or Life Sciences and have at least two years of relevant experience in the biopharmaceutical or pharmaceutical industries. **

Salary

Base: $65,000.00 - $104,650.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Root cause analysis investigations
  • Regulatory compliance assurance
  • Quality nonconformance reporting
  • Cross-functional team leadership
  • Risk assessment and impact analysis
  • Corrective and preventative actions
  • Subject Matter Expert for audits

Nice-to-have

  • Experience with enterprise systems
  • Data collection and trend analysis
  • Internal and external regulatory audits
  • Process improvements in manufacturing
  • Effective communication skills
  • Software applications for data analysis
  • Compliance issue recognition

Key Requirements

  • Minimum 2 years relevant experience
  • Bachelor's degree required
  • Preferred degree in Engineering or Life Science
  • Experience in Cell/Gene therapy or Biopharmaceutical industry
  • Ability to interpret scientific and regulatory documents

Work Rights

Not specified

Tailored Resume

Cover Letter