Regulatory Affairs Specialist

Job Title: Regulatory Affairs SpecialistREMOTEContract: 1 Year and Possibility of ExtensionClient is seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation, including EU MDR Class IIa readiness and technical documentation.This role is a hand-on, execution-focused contractor position responsible for reviewing technical documentation, ensuring regulatory compliance, authoring submission materials, and supporting documentation regulatory strategies across US, EU and global markets. The contractor will work cross-functionally with R&D, clinical, project management and quality teams.Work hours: 8 – 4 pm EST, 20-40 hr/week, depending on project statusSpecific Skills Needed: 510k writer,Years of Experience: 5-10 years+ of global medical device regulatory experienceReason for request (Example: project base, staff augmentation, replacement or other).Project based staff augementation for a specialized Global Health authority submission.GENERAL FUNCTIONClient is seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation, including EU MDR Class IIa readiness and technical documentation.This role is a hand-on, execution-focused contractor position responsible for reviewing technical documentation, ensuring regulatory compliance, authoring submission materials, and supporting documentation regulatory strategies across US, EU and global markets. The contractor will work cross-functionally with R&D, clinical, project management and quality teams.MAJOR DUTIES AND RESPONSIBILITIES•FDA 510(k) submissionoConduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliancePerform detailed regulatory gap assessments a Products FDA requirements (21 CFR Parts 807, 820, and applicable FDA guidance documents)Author, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format,Lead submission lifecycle activities, including:Acceptance Review support (RTA readiness)Substantive Review coordinationDrafting and submission of responses to FDA requests for Additional Information, Interactive review communicationsUpdating submission content and modules as requiredInterface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process.Provide regulatory leadership through FDA clearance.•EU MDR Technical Documentation SupportConduct EU MDR readiness assessment aligned with Notified Body expectations and conformity assessment requirements.Perform critical review and gap analysis of EU MDR technical fileProvide Cliented recommendations to ensure audit-readiness and Notified Body acceptanceLead or support submission to obtain CE Mark•Health Canada submissionPerform regulatory strategy and classification confirmation, including Medical Device License (MDL) pathway and Summary of Safety and Effectiveness (SSOR) readiness assessmentAuthor and compile complete Canadian submission dossiers in accordance with Health Canada structure and requirements.Support review process, including preparation, and coordination of responses to Health Canada information requests.•Global Regulatory Strategy and AdvisoryDevelop and maintain a harmonized global regulatory dossier to enable efficient market expansion.Define and implement documentation reuse strategies across justification, including identification of gaps, risks, assumptions, and sequencing.Author a comprehensive global strategy document outlining pathways, timelines, and key risks.Provide ongoing regulatory guidance and advisory support to the Business cross-functional teams to ensure compliance and execution alignment.Lead or support global regulatory submissions as needed.BASIC QUALIFICATIONS•Bachelor’s degree in engineering, life sciences, regulatory affairs, legal or a related field•5-10 years+ of global medical device regulatory experience•Proven experience preparing, writing and submitting FDA 510k submissions (end to end)•Experience with ophthalmic devices, capital equipment, diagnostic devices, software in medical devices, cybersecurity•Strong working knowledge of: FDA regulations (21 Parts 807, 820) FDA guidance documents and eStar requirementsExperience with Canadian regulations, EU MDR (2017/745) including Class lla, Tech docs Annex ll/lll•Demonstrated ability to work independently as a contractor in a fast-paced environmentPREFERRED QUALIFICATIONS•Experience filing medical device submissions in China and other countries•Experience with audiology devices•Experience with artificial-intelligence enabled devicesSkills & competenciesStrong technical writing and documentation skillsAbility to translate complex technical information into regulatory submissionsDetail-oriented with strong organization skillsEffective communicator across technical and non-technical stakeholdersAbility to manage multiple deliverables and timelines