GMP Document Control Specialist - QA & Compliance

A leading OTC drug manufacturing company in Daytona Beach, Florida is seeking a detail-oriented Document Control Specialist to support Quality and Regulatory operations. Responsibilities include reviewing batch records, maintaining controlled documents, and preparing documentation for audits. Candidates should have 1-3 years in a GMP-regulated environment and a high school diploma or GED. This full-time role offers a compensation range of $18–20 per hour. #J-18808-Ljbffr