# Hire the best remote FDA Submissions employees

Discover 63 remote FDA Submissions workers who are looking for their next full-time, part-time or freelance opportunity on Himalayas.

Source: https://himalayas.app/talent/fda-submissions

## 63 remote workers

| Person | Role | Location | Salary expectations | Intro |
| --- | --- | --- | --- | --- |
| [Lisa Whitman](https://himalayas.app/@lisawhitman861) | Quality Assurance | United States | 75k+ USD | I lead medical device quality systems, regulatory compliance, audits, and CAPA programs. |
| [Katron Owens](https://himalayas.app/@katronowens) | Regulatory Affairs Specialist | United States | 91k+ USD | I build compliant regulatory submissions and publishing systems for pharmaceutical and medical device products. |
| [Tyler Keady](https://himalayas.app/@tylerkeady) | Regulatory Affairs Associate | United States |  | Detail-oriented Regulatory Affairs professional with FDA compliance expertise. |
| [Sakshi Mandaliya](https://himalayas.app/@sakshimandaliya) | Regulatory Affairs Specialist | United States | 90k+ USD | I support FDA submissions, regulatory intelligence, and GMP compliance improvements. |
| [Kimberly Discar](https://himalayas.app/@kimberlydiscar) | Regulatory Specialist | United States | 115k+ USD | I deliver compliant global regulatory submissions and validated systems for biotech products. |
| [Brittney Bender](https://himalayas.app/@brittneybender) | Regulatory Affairs Specialist | United States |  | I lead FDA 510(k) strategy and global medical device regulatory submissions. |
| [Pruthvi Raj User](https://himalayas.app/@pruthvirajuser1) | Regulatory Affairs Specialist | United States | 80k+ USD | Regulatory Affairs Specialist at Calimontex Technologies LLC supporting 510(k) submissions for Class II/III medical devices. |
| [TRACY PARKER](https://himalayas.app/@tracyparker) | Regulatory Affairs Specialist | United States |  | Experienced Regulatory Operations Specialist with expertise in eCTD submissions. |
| [Sona Bhardwaj](https://himalayas.app/@sonabhardwaj) | Regulatory Affairs Specialist | United States | 60k+ USD | I build FDA regulatory strategies and quality documentation for medical devices, clinical studies, and pharmaceuticals. |
| [Christy Ngo](https://himalayas.app/@christyngo) | Regulatory Affairs Specialist | United States |  | I’m a Regulatory Affairs Specialist ensuring FDA-compliant product labeling and submissions. |
| [Joseph Ortiz](https://himalayas.app/@josephortiz2) | Regulatory Affairs Consultant | United States | 60k+ USD | I support FDA regulatory planning for biopharmaceutical, medical device, and digital health products. |
| [Mercy Evangeline Lankapalli](https://himalayas.app/@mercyevangelinelanka) | Regulatory Affairs Specialist | France |  | Detail-oriented Drug Regulatory Affairs professional with 4+ years experience. |
| [Avni Bell](https://himalayas.app/@avnibell) | Regulatory Affairs Specialist | United States | 60k+ USD | Regulatory affairs professional at LabConnect who supported IND submissions and quality-controlled audit-ready documentation. |
| [Timothy Cowart](https://himalayas.app/@timothycowart) | Senior Specialist | United States |  | Senior regulatory and quality specialist improving medical devices from design controls to global submissions. |
| [Sona Bhardwaj](https://himalayas.app/@sonabhardwaj1) | Regulatory Affairs Specialist | United States |  | Regulatory affairs professional at GE HealthCare who evaluated an AI-based SaMD pathway and prepared FDA Q-Sub questions. |
| [Ashish Baghel](https://himalayas.app/@ashishbaghel) | Regulatory Affairs Specialist | United States |  | Regulatory Affairs professional with expertise in formulation development. |
| [Prasanthi Malapati](https://himalayas.app/@prasanthimalapati) | Regulatory Medical Writer | United States |  | I author submission-ready clinical regulatory documents for global biologics, immunology, and infectious disease programs. |
| [Anupama Wenzel](https://himalayas.app/@anupamawenzel) | Regulatory Affairs Specialist | United States | 160k+ USD | Senior Regulatory Affairs Specialist at Class III med device company, FDA PMA and MDR device dossiers regulatory submissions. |
| [Payal Lanje](https://himalayas.app/@payallanje) | Regulatory Affairs Specialist | United Kingdom | 30k+ GBP | Regulatory Affairs Specialist with Capgemini FMCG artwork compliance experience and IQVIA dossier submissions for FDA and EMA. |
| [Nila Sankpal](https://himalayas.app/@nilasankpal) | Global Regulatory Affairs Director | Germany |  | Seasoned Global Regulatory Leader with expertise in FDA and EMA processes. |

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To contact someone, message them from their profile with a Himalayas employer account: [Hire on Himalayas](https://himalayas.app/hire).