Investigator - Lenti

J&J FAMILY OF COMPANIES

Raritan, New Jersey, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
Not specified (assumed on-site based on job location)
Root cause analysis investigations
Regulatory compliance assurance
Quality nonconformance reporting
Johnson & Johnson is seeking an Investigator for their Lenti team in Raritan, NJ, to lead cross-functional investigations, conduct risk assessments, and implement corrective measures to improve compliance within their pharmaceutical operations. The ideal candidate will possess a minimum of a Bachelor’s degree in Engineering or Life Sciences, along with relevant experience in the pharmaceutical or biopharmaceutical industry

Job Summary

  • Johnson & Johnson is committed to building a world where complex diseases are prevented, treated, and cured through healthcare innovation.
  • The Investigator will lead investigations to identify root causes, conduct risk assessments, and recommend corrective actions to maintain quality standards.
  • The role involves ensuring regulatory compliance, supporting audits, and driving process improvements to enhance safety, efficiency, and cost-effectiveness.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Investigator for their Lenti team in Raritan, NJ, to lead cross-functional investigations, conduct risk assessments, and implement corrective measures to improve compliance within their pharmaceutical operations. The ideal candidate will possess a minimum of a Bachelor’s degree in Engineering or Life Sciences, along with relevant experience in the pharmaceutical or biopharmaceutical industry.

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 assessments and impact analysis
  • Corrective and preventative measures

Nice-to-have

  • Experience with eLIMS and SAP
  • Internal and external regulatory audits
  • Data analysis and trend coordination
  • Effective communication skills
  • Process improvement implementation
  • Subject Matter Expert during audits

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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