Global Regulatory Specialist - Registration & Compliance

Arxada

Northern (KY)

Hybrid

USD 84,000 - 102,000

Full time

14 days+
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Benefits offered by this job

401(k) plan
Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
Paid time off
Paid holidays
Paid sick leave

Job summary

Arxada is seeking a Regulatory Specialist within our Professional Hygiene Regulatory Team to help ensure product compliance and timely registrations in North America. Based in Morristown, NJ or Alpharetta, GA, you will collaborate with R&D, marketing and external agencies to drive registrations and support audits while upholding our standards of regulatory excellence.

You will prepare and monitor regulatory submissions, liaise with agencies, maintain documentation, and identify opportunities to

Qualifications

  • Degree in Life Sciences, Chemistry, or related discipline or equivalent regulatory experience.
  • Knowledge of FIFRA regulations, EPA pesticide registrations, and North American requirements.
  • Strong written and verbal communication with attention to detail.

Responsibilities

  • Prepare, submit, and monitor regulatory applications and registrations.
  • Liaise with regulatory agencies, customers, and internal teams to resolve issues.
  • Support audits, inspections, and regulatory reviews with accurate documentation.
  • Collaborate with R&D and cross-functional teams to improve processes.

Skills

Communication
Organizational Skills
Stakeholder Management
Attention to Detail

Education

Bachelor's degree in Life Sciences or Chemistry or related

Tools

Microsoft Office
Registration management systems

Job description

Arxada is seeking a Regulatory Specialist within our Professional Hygiene Regulatory Team to help ensure product compliance and timely registrations in North America. Based in Morristown, NJ or Alpharetta, GA, you will collaborate with R&D, marketing and external agencies to drive registrations and support audits while upholding our standards of regulatory excellence.

You will prepare and monitor regulatory submissions, liaise with agencies, maintain documentation, and identify opportunities to

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