Quality EQMS & Training Coordinator

ADP; Buford (GA); On-site; USD 55,000 - 75,000; Full time

Job summary

ADP in Buford, GA is seeking a detail-oriented Document Control professional to manage EQMS (QCBD) and oversee the document control process in compliance with medical device regulations. You will coordinate training, maintain revision histories, issue ECNs, archive quality records, and support FDA inspections while contributing to process improvements across the department.

The role requires 3–5 years of relevant experience and proficiency with Microsoft Word and Excel; a high school diploma is

Qualifications

• Detail oriented, accurate, and efficient.
• Must have strong organizational skills.
• Proficient in Microsoft Word and Excel.
• 3–5 years of relevant work experience.

Responsibilities

• Coordinate changes to controlled documents and revisions.
• Track and release controlled documents to ensure current versions.
• Process Engineering Change Notices (ECNs) per regulatory requirements.
• Maintain revision history and archival of ECNs and revisions.
• Coordinate training notifications and maintain training logs.
• Support FDA inspections with back room audit activities.

Skills

Detail oriented

Organization skills

Communication skills

multitask

Flexibility

Independent work

Education

High School Diploma

Associate degree or higher

Tools

Microsoft Word

Microsoft Excel

Job description

ADP in Buford, GA is seeking a detail-oriented Document Control professional to manage EQMS (QCBD) and oversee the document control process in compliance with medical device regulations. You will coordinate training, maintain revision histories, issue ECNs, archive quality records, and support FDA inspections while contributing to process improvements across the department.

The role requires 3–5 years of relevant experience and proficiency with Microsoft Word and Excel; a high school diploma is