Qc Investigation Support Specialist

J&J FAMILY OF COMPANIES

Raritan, New Jersey, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
Hybrid
Bachelor's degree required
Two years qc lab experience
Cgmp and fda guidance knowledge
Johnson & Johnson is seeking a QC Investigation Support Specialist for its Innovative Medicine division in Raritan, NJ. The role involves investigating deviations in Quality Control laboratories for cell therapy products, requiring strong technical writing skills and knowledge of GMP practices

Job Summary

  • The role involves investigating deviations to support Quality Control testing laboratories for cell therapy products in a controlled GMP environment.
  • Candidates must apply strong technical writing skills to draft clear deviation and investigation documentation while collaborating with cross-functional teams.
  • Employees are eligible for comprehensive benefits including up to 480 hours of parental leave, 13 days of holiday pay, and a 401(k) savings plan.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a QC Investigation Support Specialist for its Innovative Medicine division in Raritan, NJ. The role involves investigating deviations in Quality Control laboratories for cell therapy products, requiring strong technical writing skills and knowledge of GMP practices.

Salary

Base: $65,000.00 - $104,650.00; Bonus/Equity: Not specified; Benefits: Retirement plan, 401(k), vacation, sick time, parental leave

Skills & Requirements

Must-have

  • Bachelor's degree required
  • Two years QC lab experience
  • cGMP and FDA guidance knowledge
  • Technical writing for investigations
  • Good Documentation Practices (GDP)
  • Deviation risk assessment skills

Nice-to-have

  • Cell therapy QC assay knowledge
  • QEM system familiarity
  • Compendial standards expertise
  • Inspector interaction experience
  • Cross-functional presentation skills

Key Requirements

  • Minimum Bachelor's degree
  • 2+ years relevant work experience
  • Knowledge of cGMP and FDA/EU guidance
  • Proficiency in Good Documentation Practices
  • Ability to accommodate shift schedule and overtime

Work Rights

Not specified

Tailored Resume

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