Regulatory Affairs Specialist - Scottsdale, AZ

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 ...

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. · ...

+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+ ...

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 ...

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 ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week at our Exton PA. · The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, · developing strategies, · authoring, · ...

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 ...

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. · ...

Central has an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join their team. · ...

The Government Affairs Specialist will be a key player in shaping policy and advocating for the interests of the AAA Mountain West Group (MWG). As the government affairs contact for this region, you will help develop and implement advocacy strategies, effectively build relationsh ...

The Government Affairs Specialist will be a key player in shaping policy and advocating for the interests of the AAA Mountain West Group · Assist the government affairs team in crafting and executing strategies tailored to state legislatures. · Partner with state lobbyists to ed ...

BioLab Holdings is seeking an accomplished Regulatory Affairs leader with hands-on regulatory experience to architect and drive regulatory strategy for complex products. · ...

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 ...

This role will proactively engage with state economic development agencies, governors' offices, legislators and federal agencies to identify pursue and negotiate grants tax credits and incentive programs. · ...

Lead day-to-day efforts securing state and federal funding for large-scale manufacturing and energy projects. · Coordinate funding applications · Develop incentive strategies · ...

Prepares regulatory applications and reviews communications to ensure they adhere to applicable regulatory standards. Maintains medical device regulations and supports product release process. · ...

This role will proactively engage with state economic development agencies, governors' offices, legislators, and federal agencies to identify, pursue, and negotiate grants, tax credits, and incentive programs. · Coordinate funding applications. · Develop incentive strategies. · < ...

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 ...

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. · ...

We're looking for a detail-oriented Data Privacy Specialist to help strengthen and evolve our privacy program as we grow. This role ensures our clinical and corporate operations meet healthcare, privacy, and data protection standards. · ...