QC Documentation Specialist
United Pharma
Our client is seeking an experienced Technical Writer with a strong chemistry and pharmaceutical laboratory background. 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 #J-18808-Ljbffr
Vacancy posted 3 days ago
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