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JOB SUMMARY:
The Regulatory Supervisor position plays a key role in ensuring compliance with a variety of regulations within the industry. The Regulatory Supervisor is responsible for preparing, amending, and maintaining product registration for all product categories within our chemical manufacturing division and staying up to date with regulatory changes. This role works closely with the Technical Services, ZEE Sales organization and Vincit ERP support to ensure accuracy and compliance.
EDUCATION:
Required: Bachelor’s degree in a related field (Chemistry, Biology, Biochemistry, Polymer Science, Regulatory Affairs, etc.)
EXPERIENCE:
Required: 5-7 years of experience working in regulatory affairs.
Preferred: 7+ years of experience working with US EPA, FIFRA, and FDA authorities regarding new and existing product registrations and label amendments in US, Canada and Mexico.
POSITION REQUIREMENT(S): Specialized Skills/License/Certification
Required: High attention to detail and organizational skills. Ability to multitask and problem solve, system and process oriented, ability to comprehend federal and state regulations, and effective communication skills. Ability to work independently and adhere to strict deadlines. Knowledge of regulatory requirements pertaining to industrial chemicals. Proficient in MS Office Applications (Outlook, PowerPoint, Outlook, Excel, Word). Experienced in data collection, analysis, and documentation. Strong understanding of laws and regulations pertaining to chemical regulatory management.
CORE COMPETENCIES (Essential Job Functions)
1. Responsible for managing product registrations for US, Canada and Mexico, encompassing preparation and submission of state and federal documents, as well as the upkeep of current registrations and any necessary amendments.
2. Create and execute regulatory strategies aligned with business goals to facilitate the achievement of organizational objectives.
3. Assess regulatory compliance of label modifications and technical and marketing materials.
4. Maintain US EPA and State EPA product registrations.
5. Maintain FDA establishment and product listings.
6. Maintaining knowledge on amended, current and future regulation changes as it relates.
7. Collaborate with multiple departments as needed to ensure regulatory compliance.
8. Partner with necessary third-party consultants.
9. Manage GLP testing to support product registration.
10. Supervise Regulatory Specialists assigned to Regulatory team. Handle all functions associated with team leadership and personnel management.
11. Proactively identify any areas of business risk and prepare advisement for senior leadership.
12. Perform other duties as assigned.
VIN123
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