Documentation Specialist | cGMP/ISO13485 Pro

A healthcare staffing company is seeking a Documentation Specialist in Ridgefield, NJ. The role involves verifying Batch Production Records to ensure compliance with cGMP and ISO 13485 standards. Candidates should have at least 3 years of experience in a cGMP environment and a High School Diploma. Experience in the pharma or medical device industry is preferred. The position offers an hourly rate of $25-30 and is set for a 12-month assignment with potential for extension. #J-18808-Ljbffr