Senior Technical Writer

J&J FAMILY OF COMPANIES

Titusville, New Jersey, United States of America
Base: $79,000.00 - $127,650.00; bonus/equity: elig...
Hybrid
Experience working in qc laboratory as bench analyst
Demonstrated use of root cause analysis tools
Knowledge of current good manufacturing practices cgmp
Johnson & Johnson is seeking a Senior Technical Writer in Titusville, New Jersey, to lead the technical writing of GMP documents and investigations within their Quality Control operations. The ideal candidate will have a strong background in laboratory practices, technical writing, and compliance with GMP regulations

Job Summary

  • The Technical Writer is responsible for driving results by leading the technical writing of GMP documents and investigations within the NJ Stability Lab Operations.
  • This position requires completing investigations including identification of root causes while ensuring compliance with FDA, EPA, DEA, and OSHA regulations.
  • Employees are eligible for comprehensive benefits including a 401(k) savings plan, long-term incentive program, and up to 480 hours of parental leave.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Technical Writer in Titusville, New Jersey, to lead the technical writing of GMP documents and investigations within their Quality Control operations. The ideal candidate will have a strong background in laboratory practices, technical writing, and compliance with GMP regulations.

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: 401(k), pension, vacation, sick time, holiday pay, parental leave

Skills & Requirements

Must-have

  • Experience working in QC laboratory as bench analyst
  • Demonstrated use of root cause analysis tools
  • Knowledge of current Good Manufacturing Practices cGMP
  • Proficiency with Microsoft Office applications
  • Experience with Quality Systems Trackwise Docspace TruVault

Nice-to-have

  • Creativity regarding basic problem solving
  • Ability to positively influence peers
  • Pro-active change agent mindset
  • Optimistic attitude towards work
  • Capability to develop improvement ideas

Key Requirements

  • Experience working in QC laboratory as bench analyst
  • Knowledge of compendial USP EP JP requirements
  • Advanced technical writing skills
  • Ability to work independently on assignments

Work Rights

Not specified

Tailored Resume

Cover Letter