Senior Technical Writer

What you’d do

Write and edit GMP documents for NJ Stability Lab Operations, including laboratory investigations, SOPs, and validation protocols and reports. Full time role requiring root cause analysis and QC lab experience. Found on the employer's careers page on Oct 20, 2026. Apply through the link.

You’ll need

• QC laboratory bench analyst experience
• Technical writing of GMP documents and investigations
• Knowledge of HPLC, Dissolution, IR, Karl Fischer
• Root cause analysis tools (Kepner-Tregoe, Fishbone, 5-Why)
• Knowledge of FDA, EPA, DEA, OSHA regulations