Global Regulatory Affairs Specialist (Food & Pharma)

Darling Ingredients Inc.; Irving (TX); On-site; USD 80,000 - 120,000; Full time

Benefits offered by this job

401(k)

Health insurance

Dental insurance

Vision insurance

Paid time off

Job summary

Rousselot, the Darling Ingredients health brand, seeks a Regulatory Affairs professional to manage regulatory documentation, track regulatory changes, and support the needs of food, food supplements, pharmaceutical, biomedicals and animal by-product customers.

You will maintain supplier compliance for the USA and prepare FDA affidavits, Letters of Guarantee and Prop 65 statements, collaborating with project teams to ensure timely, compliant results.

Qualifications

• Experience in regulatory documentation and compliance.
• Experience with FDA submissions and shipments.
• Ability to maintain USA supplier compliance and regulatory records.

Responsibilities

• Maintains accurate regulatory statements to ensure global compliance.
• Prepares regulatory documents for customers (Letters of Guarantee, Prop 65).
• Prepares FDA shipment affidavits and regulatory submissions.
• Represents regulatory affairs on project teams and provides guidance.
• Communicates progress on regulatory projects and ensures team objectives are met.
• Completes and manages Customer Quality Questionnaires.
• Follows food safety procedures and promotes a strong food safety culture.

Skills

Regulatory affairs

Regulatory documentation

FDA compliance

Team collaboration

Job description

Rousselot, the Darling Ingredients health brand, seeks a Regulatory Affairs professional to manage regulatory documentation, track regulatory changes, and support the needs of food, food supplements, pharmaceutical, biomedicals and animal by-product customers.

You will maintain supplier compliance for the USA and prepare FDA affidavits, Letters of Guarantee and Prop 65 statements, collaborating with project teams to ensure timely, compliant results.