QC Documentation Specialist

Responsibilities: Write and own deviation investigations and quality documentation Document hypothesis testing and retesting activities Translate technical laboratory information into clear documentation Work with QC teams on analytical and laboratory investigations

Requirements: 5 to 7+ years of relevant experience Strong technical writing experience in a GMP environment Chemistry background with HPLC and GC experience Has personally written deviation or OOS investigations, including hypothesis testing and retesting Bachelor's degree in Chemistry or related field preferred