Regulatory Specialist - Scottsdale, AZ
1 month ago

Job summary
We are seeking a highly organized and detail-oriented Regulatory Specialist to support regulatory and quality documentation operations across 10X Health's supplement portfolio.This role focuses on maintaining audit-ready documentation, routing product and marketing assets for approval, and supporting the organization of supplier and product files.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. This position requires a minimum of five years medical device regulatory experi ...
5 days ago
+Job summary · The Regulatory Affairs Specialist role is responsible for preparing and submitting documentation for FDA 510(k) submissions.++•Ability to work in a fast paced collaborative team environment+•Ability to handle multiple projects and coordinate cross functional teams+ ...
1 week ago
The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and helps support the work associated with obtaining government approval for product imports into global markets. · ...
1 month ago
The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions. · ...
6 days ago
The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and help support the work associated with obtaining government approval for product imports into global markets. Thi ...
1 month ago
The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and help support the work associated with obtaining government approval for product imports into global markets.The ...
1 week ago
The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · ...
3 weeks ago
The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · We are seeking a highly mot ...
4 weeks ago
We are looking for a detail-oriented research professional to join our team. · Support regulatory submissions (IRB) · , Maintain regulatory binders and essential documents · , Cordinate study operations: screening · , Collaborate closely with investigators · ...
1 month ago
Arizona Cardiovascular Research Center is growing and we're looking for a detail-oriented patient-centered research professional to join our team. · ...
1 month ago
Central has an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join their team. · ...
1 month ago
BioLab Holdings is seeking an accomplished Regulatory Affairs leader with hands-on regulatory experience to architect and drive regulatory strategy for complex products. · ...
1 month ago
We have an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join our team This position reports to the Sr. · Director, FDA Regulatory Affairs & Food Safety and will support Central animal food facilities. · The position includes interacting ...
1 month ago
Prepares regulatory applications and reviews communications to ensure they adhere to applicable regulatory standards. Maintains medical device regulations and supports product release process. · ...
1 month ago
We are seeking motivated professionals with experience in healthcare claims appeals and reimbursement for the Healthcare Appeals & Compliance Specialist role. · ...
1 week ago
Join Vanguard's mission to protect the financial system as a Financial Crimes Specialist in AML Investigations. Detect and prevent financial crime, safeguard clients and firm integrity. · ...
1 month ago
At Vitalant our work saves lives—and the strength of our operations makes that possible. We are a mission-driven organization committed to continuous improvement innovation and the highest standards of quality and compliance. · ...
1 month ago
The Routing and Siting Specialist plays a key role in balancing technical, environmental, · and social factors to determine appropriate locations for infrastructure projects. · Route and Site Selection: Identify and evaluate potential routes or sites for projects, · considering f ...
6 days ago
The Senior Procurement Specialist supports strategic sourcing initiatives by managing procurement projects, supplier sourcing, cost analysis and risk mitigation in a regulated manufacturing environment. · ...
3 weeks ago
This role involves leading sourcing and procurement projects for medical device components. · ...
3 weeks ago