Specialist Quality Compliance Drug Enforcement Administration (DEA)

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

Role: Specialist Quality Compliance DEA at Johnson & Johnson

supporting controlled substance regulatory adherence across sites. Responsibilities include compiling DEA reports, supporting audits, inventory reconciliation, reporting quota consumption, managing documentation, facilitating regulatory inspections, and delivering compliance training. The position emphasizes collaboration with security and other departments to ensure secure manufacturing environments and adherence to federal, state, and local regulations.

Qualifications

Minimum of an associate degree or equivalent, with at least 2 years of relevant experience in pharmaceutical or chemical manufacturing environments. Skills required include interpreting government regulations, preparing reports, analyzing data, and proficiency with software tools. Knowledge of cGMP, quality assurance, safety, and environmental standards is essential.

High-Value specifics

Focus on controlled substances compliance, DEA regulations, inventory reconciliation, and audits. The role involves up to 10% domestic travel and requires understanding of regulatory standards such as FDA, EPA, OSHA, and DEA.

Preferred skills

Audit management, compliance trend analysis, process optimization, and regulatory environment expertise. The role offers development opportunities in leadership and networking within J&J's global controlled substance organization.