Specialist Quality Compliance Drug Enforcement Administration; DEA)

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.

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.

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.

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.