Regulatory Affairs Specialist — GMP, Customer‑Centric Support

TREATT NORTH AMERICA; Lakeland (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

TREATT NORTH AMERICA is seeking a Regulatory Affairs Specialist to interpret regulatory changes and ensure product safety, efficacy, and compliance for Treatt products. The role supports customers and the commercial team while maintaining regulatory documentation.

You will work with GMP, HACCP, JD Edwards/SAP, and MS Office, collaborating across departments to improve quality and efficiency in a customer‑centric environment.

Qualifications

• Education: Associate degree or HS Diploma with 5 years industry experience.
• GMP and HACCP knowledge are required.
• Familiarity with ERP systems and Microsoft Office applications.
• Experience with customer inquiries and regulatory documentation is preferred.

Responsibilities

• Complete Customer Questionnaires and product questions within 24 hours of receipt.
• Prepare product documentation per current regulations.
• Communicate with internal and external customers for problem solving.
• Provide product support to the commercial team.
• Maintain regulatory data in ERP systems and document management.

Skills

GMP knowledge

HACCP knowledge

Strong communication

Team orientation

Organizational skills

Self-directed

Ability to follow instructions

Education

Associate degree or HS Diploma with 5 yrs experience

Tools

JD Edwards

SAP

Microsoft Office

3rd party portals

Job description

TREATT NORTH AMERICA is seeking a Regulatory Affairs Specialist to interpret regulatory changes and ensure product safety, efficacy, and compliance for Treatt products. The role supports customers and the commercial team while maintaining regulatory documentation.

You will work with GMP, HACCP, JD Edwards/SAP, and MS Office, collaborating across departments to improve quality and efficiency in a customer‑centric environment.