Knowledge of current good manufacturing practices cgmp
Johnson & Johnson is seeking a Senior Technical Writer to support their Quality Control laboratory operations in Titusville, New Jersey. The role involves writing and reviewing GMP documents, conducting investigations, and ensuring compliance with regulatory standards while fostering an inclusive work environment
Job Summary
The role involves leading the technical writing of GMP documents and investigations within the NJ Stability Lab Operations at Johnson & Johnson.
Candidates must demonstrate strong written communication skills and knowledge of FDA, EPA, DEA, and OSHA regulations.
Employees are eligible for comprehensive benefits including a 401(k) savings plan, long-term incentive programs, and up to 480 hours of parental leave.
Matching Summary
Match Score: 85
Johnson & Johnson is seeking a Senior Technical Writer to support their Quality Control laboratory operations in Titusville, New Jersey. The role involves writing and reviewing GMP documents, conducting investigations, and ensuring compliance with regulatory standards while fostering an inclusive work environment.
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 in QC laboratory as bench analyst
Root cause analysis tools like Kepner-Tregoe
Knowledge of current Good Manufacturing Practices cGMP
Proficiency with Quality Systems Trackwise or Docspace
Ability to write detailed SOPs and validation reports
Nice-to-have
Creativity in problem solving and troubleshooting
Pro-active change agent mindset
Positive influence on peers and team members
Mentorship capabilities for new writers
Key Requirements
QC laboratory bench analyst experience required
Advanced technical writing skills required
Proficiency with Microsoft Office applications required