Remote Regulatory Affairs Supervisor

Cardinal Health; Trenton (NJ); Remote; USD 80,000 - 117,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off

401k savings plan

Health savings account (HSA)

Disability coverage

Work-Life resources

Job summary

Cardinal Health is seeking a Supervisor, Regulatory Affairs to lead regulatory programs across labeling, listings, and compliance for pharma, medical device, and cosmetics portfolios. You will guide cross-functional teams, maintain SOPs, and ensure alignment with FDA standards while protecting supply chain integrity.

The role emphasizes collaboration with QA, legal, and operations to minimize risk and drive compliant product listings, with a nationwide remote work setup and a competitive

Qualifications

• 4–8 years of experience in pharmaceutical/medical device Quality Assurance or Regulatory Affairs.
• Bachelor’s degree in a related scientific/technical field.
• Familiarity with FDA Compliance Policy Guides (CPGs), 21 CFR 11, and USP standard testing.
• Experience with Kallik, FACTS, or Veeva Vault QMS.

Responsibilities

• Coordinate and supervise daily labeling and listing activities.
• Develop, implement, and enforce SOPs to support regulatory compliance.
• Collaborate with QA, packaging operations, and legal groups to resolve issues.
• Oversee FDA submissions, drug listing operations, and regulatory database integrity.

Job description

Cardinal Health is seeking a Supervisor, Regulatory Affairs to lead regulatory programs across labeling, listings, and compliance for pharma, medical device, and cosmetics portfolios. You will guide cross-functional teams, maintain SOPs, and ensure alignment with FDA standards while protecting supply chain integrity.

The role emphasizes collaboration with QA, legal, and operations to minimize risk and drive compliant product listings, with a nationwide remote work setup and a competitive