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 ...
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 ...
Regulatory Supervisor
Chattanooga, TN · On-site
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 ...
Regulatory Supervisor
Chattanooga, TN · On-site
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 ...
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · On-site
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · On-site
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
International Regulatory Affairs Specialist
Brooklyn Park, MN · Hybrid
$90K - $100K/yr
This role supports product registration, regulatory strategy, and compliance activities to enable global market access. This includes reviewing product chemistry, toxicology, and efficacy data, as ...
International Regulatory Affairs Specialist
Brooklyn Park, MN · Hybrid
$90K - $100K/yr
This role supports product registration, regulatory strategy, and compliance activities to enable global market access. This includes reviewing product chemistry, toxicology, and efficacy data, as ...
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · On-site
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
Quick apply
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · On-site
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · Hybrid
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
Clinical Research Coordinator I (Temporary/Part-Time)
Seattle, WA · Hybrid
$26.44 - $31.25/hr
Product Registrations (International) * Identify regulatory requirements for product registrations worldwide. * Review analytical and clinical data against country regulatory requirements and ...
Bilingual Documentation Specialist (Eng/Spa)
Fort Lauderdale, FL · On-site
$19/hr
This role focuses on preparing, organizing, and tracking documents required for product registrations and international customers . The ideal candidate is detail-oriented, organized, and comfortable ...
Quick apply
Bilingual Documentation Specialist (Eng/Spa)
Fort Lauderdale, FL · On-site
$19/hr
This role focuses on preparing, organizing, and tracking documents required for product registrations and international customers . The ideal candidate is detail-oriented, organized, and comfortable ...
Bilingual Documentation Specialist (English/Spanish)
Davie, FL · On-site
$19/hr
This role focuses on preparing, organizing, and tracking documents required for product registrations and international customers . The ideal candidate is detail-oriented, organized, and comfortable ...
Quick apply
Bilingual Documentation Specialist (English/Spanish)
Davie, FL · On-site
$19/hr
This role focuses on preparing, organizing, and tracking documents required for product registrations and international customers . The ideal candidate is detail-oriented, organized, and comfortable ...
Specialist, Regulatory Affairs
Santa Clarita, CA · On-site
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Quick apply
Specialist, Regulatory Affairs
Santa Clarita, CA · On-site
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Specialist, Regulatory Affairs (Santa Clarita)
Santa Clarita, CA · On-site
$39.61 - $43.57/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Specialist, Regulatory Affairs (Santa Clarita)
Santa Clarita, CA · On-site
$39.61 - $43.57/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
Specialist, Regulatory Affairs
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Quick apply
Specialist, Regulatory Affairs
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Specialist, Regulatory Affairs (Santa Clarita)
$39.61 - $43.57/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Specialist, Regulatory Affairs (Santa Clarita)
$39.61 - $43.57/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Product Registration & Regulatory Documentation Support * Coordinate documentation packages required for international product registrations and market entry activities. * Collect, organize, and ...
Product Registration & Regulatory Documentation Support * Coordinate documentation packages required for international product registrations and market entry activities. * Collect, organize, and ...
Regulatory Affairs Specialist III
Plano, TX · On-site
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
Regulatory Affairs Specialist III
Plano, TX · On-site
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
Specialist, Regulatory Affairs
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Specialist, Regulatory Affairs
$39.61 - $43.27/hr
Prepare international documentation to support product registration internationally * File all new product notifications and update current notifications with Health Canada * Maintain regulatory ...
Responsible for ensuring that our products comply with all regulatory requirements in Colombia ... This position reports to the Manager, Registration and Regulatory Compliance Latin America Northern ...
Responsible for ensuring that our products comply with all regulatory requirements in Colombia ... This position reports to the Manager, Registration and Regulatory Compliance Latin America Northern ...
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical ...
Executes and ensures timely product registration and release for distribution. * As the Regulatory Affairs functional lead, oversee and optimize processes and team efforts to obtain and maintain ...
Executes and ensures timely product registration and release for distribution. * As the Regulatory Affairs functional lead, oversee and optimize processes and team efforts to obtain and maintain ...
Executes and ensures timely product registration and release for distribution. * As the Regulatory Affairs functional lead, oversee and optimize processes and team efforts to obtain and maintain ...
Executes and ensures timely product registration and release for distribution. * As the Regulatory Affairs functional lead, oversee and optimize processes and team efforts to obtain and maintain ...
Product Registration information
See salary details
$41.5K - $52.7K
0% of jobs
$52.7K - $63.9K
0% of jobs
$63.9K - $75K
1% of jobs
$75K - $86.2K
12% of jobs
$94.3K is the 25th percentile. Wages below this are outliers.
$86.2K - $97.4K
17% of jobs
The median wage is $108.6K / yr.
$97.4K - $108.6K
20% of jobs
$108.6K - $119.8K
18% of jobs
$126.4K is the 75th percentile. Wages above this are outliers.
$119.8K - $131K
12% of jobs
$131K - $142.1K
10% of jobs
$142.1K - $153.3K
7% of jobs
$153.3K - $164.5K
3% of jobs
$41.5K
$112.9K
$164.5K
How much do product registration jobs pay per year?
What is the difference between Product Registration vs Quality Assurance Specialist?
| Aspect | Product Registration | Quality Assurance Specialist |
|---|---|---|
| Required Credentials | Regulatory knowledge, certifications in compliance | Quality management certifications, ISO standards |
| Work Environment | Regulatory agencies, compliance departments | Manufacturing, testing labs, quality departments |
| Employer & Industry Usage | Consumer goods, pharmaceuticals, electronics | Manufacturing, food production, biotech |
| Search & Comparison Intent | Understanding product compliance processes | Ensuring product quality and standards |
Product Registration involves ensuring products meet regulatory requirements and obtaining necessary approvals, while a Quality Assurance Specialist focuses on maintaining product quality through testing and process improvements. Both roles are essential in product development and compliance but serve different functions within the industry.
What are some common challenges faced in a Product Registration role, and how can I prepare to address them?
What is product registration and why is it important?
What are the key skills and qualifications needed to thrive as a Product Registration Specialist, and why are they important?

Full-time
Posted 19 days ago
Job description
It's fun to work in a company where people truly BELIEVE in what they're doing!
We're committed to bringing passion and customer focus to the business.
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
If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!