DEA Quality Compliance Specialist — Controlled Substances

Johnson & Johnson Innovative Medicine; Athens (GA); On-site; USD 85,000 - 110,000; Full time

Job summary

Johnson & Johnson is seeking a Specialist Quality Compliance DEA to ensure regulatory adherence across sites. You will compile DEA reports, support audits, conduct inventory reconciliation, report quota consumption, manage documentation, facilitate inspections, and deliver compliance training.

Collaboration with security and other departments is essential to maintain secure manufacturing environments. The role emphasizes regulatory oversight across federal, state, and local requirements and

Qualifications

• Associate degree or equivalent with at least 2 years of relevant experience in pharmaceutical or chemical manufacturing environments.
• Ability to interpret government regulations and prepare reports.
• Experience in pharmaceutical or chemical manufacturing environments.
• Knowledge of regulatory standards such as FDA, EPA, OSHA, and DEA.

Responsibilities

• Compile DEA reports and support audits.
• Conduct inventory reconciliation and report quota consumption.
• Manage regulatory documentation and facilitate inspections.
• Deliver compliance training and collaborate with security and other departments.

Skills

Regulatory interpretation

Report preparation

Data analysis

Software proficiency

cGMP knowledge

Quality systems

Safety standards

Environmental standards

Education

Associate degree

Job description

Johnson & Johnson is seeking a Specialist Quality Compliance DEA to ensure regulatory adherence across sites. You will compile DEA reports, support audits, conduct inventory reconciliation, report quota consumption, manage documentation, facilitate inspections, and deliver compliance training.

Collaboration with security and other departments is essential to maintain secure manufacturing environments. The role emphasizes regulatory oversight across federal, state, and local requirements and