Investigation Writer & CAPA Analyst (GMP/QMS)

A leading medical device company in the United States is seeking an experienced professional to conduct technical investigations and ensure compliance with industry regulations. The role involves using root cause analysis tools, collaborating with cross-functional teams, and managing CAPAs within the Veeva QMS system. The ideal candidate will have 7–8 years of experience, particularly in the Medical Device or Injectables industry, and a strong background in investigation writing and reporting. Competitive salary and development opportunities are offered. #J-18808-Ljbffr