Fda Jobs in Florida (NOW HIRING)

Former FDA experience is a plus but is not required. Location & Availability This engagement requires onsite support north of Miami, Florida . Consultants located in the Fort Lauderdale/Miami/South ...

This role coordinates and submits regulatory reports to FDA and Country/Regional competent authorities. * Engaged in the receipt, documentation, investigation, and closure/resolution of customer ...

This role coordinates and submits regulatory reports to FDA and Country/Regional competent authorities. Key Responsibilities * Engaged in the receipt, documentation, investigation, and closure ...

FDA Submissions * Independently prepare and submit: * Traditional 510(k)s * Special 510(k)s * eSTAR submissions * Letters to File * Q-Submissions * Coordinate submission content across Engineering ...

S. Food and Drug Administration (FDA). Serves as a liaison with regulatory agencies and affiliates, as well as providing regulatory guidance to address FDA questions for both investigational and ...

This role is critical to ensuring our FDA-regulated products move efficiently, compliantly, and on schedule to our retail partners. Key Responsibilities* Manage inbound international shipments (ocean ...

This role is critical to ensuring our FDA-regulated products move efficiently, compliantly, and on schedule to our retail partners. Key Responsibilities * Manage inbound international shipments ...

This role is critical to ensuring our FDA-regulated products move efficiently, compliantly, and on schedule to our retail partners. Key Responsibilities * Manage inbound international shipments ...

Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k) submissions. * Create Regulatory Master Plans for product launches. * Lead the development of new ...

Review of FDA submissions. * Assist/work with consultants as needed. * Support R&D with 510(k) submissions. * Create Regulatory Master Plans for product launches. * Lead the development of new ...

S. Food and Drug Administration (FDA). Serves as a liaison with regulatory agencies and affiliates, as well as providing regulatory guidance to address FDA questions for both investigational and ...

S. Food and Drug Administration (FDA). Serves as a liaison with regulatory agencies and affiliates, as well as providing regulatory guidance to address FDA questions for both investigational and ...

This role is responsible for ensuring compliance with FDA regulations and maintaining regulatory documentation related to manufacturing, packaging, labeling, and holding operations for dietary ...

The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality. Key Responsibilities:

Work in a regulated environment (FDA, EPA, etc.) is preferred, but not required Compliance Requirements (ES) The minimum compliance expectation for this role entails strict adherence to FDA ...

The ideal candidate will coordinate daily production activities, ensure compliance with FDA and GMP regulations, and support overall production efficiency and quality. Key Responsibilities:

FDA 21 CFR 820.30 (Design Controls) * ISO 13485 design and development requirements * Combination product regulations (21 CFR Part 4) * Maintain complete design traceability from: * User needs → ...

The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...

The ideal candidate is bilingual (English/Spanish) , organized, and has prior experience in pharmaceutical or FDA-regulated environments. Location: Miramar, FL Industry: Pharmaceutical Manufacturing ...

Position Summary The QA Technician ensures that all raw materials, in-process production, and finished products meet quality and food safety standards (GMP, SQF, FDA). This role is essential in ...