Director of Regulatory Affairs
$205k - $245kGatewell Group
Gatewell Group is a Los Angeles compliance firm working the FCC Covered List: vendor-bench diligence, origin evidence, and Conditional Approval filings for manufacturers and the US companies that buy from them. We are hiring a new Director of Regulatory Affairs. The Director coordinates operations across our regulatory practice lines (equipment authorization, Conditional Approval filings, and the evidence standards behind both), and directs every technical filing the firm makes. You would set the evidentiary standard, not inherit one. What you would do Direct the technical content of Conditional Approval filings to the FCC and the reviewing agency (DoW for robotics, DoW or DHS for inverters), including per-component BOM origin, supply-chain concentration analysis, and the officer certification package. Own agency correspondence. You are the firm's technical voice on the record. Set the evidentiary bar for Gatewell Protocol origin-evidence work, and review analyst work product against it. Advise clients on equipment-authorization strategy, including permissive-change exposure for already-authorized devices under the Class I/II restrictions and the DA 26-789 software waiver. Screen prospective filing engagements. We take only the cases we believe in, and you would hold that line with us. Who this is for Ten or more years inside FCC equipment authorization. The strongest candidates are former lead reviewers at a Telecommunication Certification Body, former FCC OET staff, or senior certification engineers at an FCC-recognized lab. You have read more failed applications than most consultants have read successful ones, and you can say precisely why they failed. Working knowledge of 47 CFR Part 2 Subpart J, the KDB publications, and the Covered List framework as it has developed since the December 2025 drone listing. You can write for a regulator. Most of this job is written. Compensation and location $205,000 to $245,000 , depending on depth of agency experience. Full-time, in-house, hybrid. You work from our Los Angeles office as the week requires. This is not a remote role. You must reside in Southern California and be authorized to work in the United States. We do not sponsor employment visas. Client and agency travel as filings require. #J-18808-Ljbffr Gatewell Group
$160k - $260k
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$130k - $160k
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At KPMG, you can become an integral part of a dynamic team at one of the worlds top tax firms. Enjoy a collaborative, future-forward culture that empowers your success. Work with KPMGs extensive network of specialists; enjoy access to our Ignition Centers, where deep industry...Full timeLocal area$110k - $135k
Manager, Global Regulatory Affairs|The Wonderful Company# Manager, Global Regulatory AffairsThe Wonderful Company | Los Angeles, CA | Legal | Associate | Full-time | Job ID: REF6319QShare* Email## Company DescriptionThe Wonderful Company is committed to offering high-quality...Full timeWork at officeRemote workWorldwide$120k - $150k
...structure, policies, standards, expectations, and accountability across CHAOS businesses. You'll report to the IT/Cybersecurity Program Director and work daily with IT, Cybersecurity, Physical Security, and Manufacturing - teams with different priorities and vocabulary;...Permanent employmentContract workWork experience placementFor subcontractorCasual workRelocation package- Gatewell Group in Los Angeles is seeking a Director of Regulatory Affairs to lead our FCC equipment-authorization practice and oversee Conditional Approval filings. You would set the evidentiary bar and direct the agency correspondence, becoming the firm’s technical voice...
$175k - $200k
...every stage of your career. Try new things, learn new skills and discover what you excel at—all from Day One.Job DescriptionThe Regulatory Administration group supports fund clients through preparation of registered investment company regulatory filings, fund governance...Work at officeLocal areaRemote workFlexible hours3 days per week- ...Team of CPC/CCS certified Compliance Auditors to ensure accurate, compliant documentation and coding practices in alignment with regulatory requirements, organizational policies, and industry standards. This role manages the execution of medical record documentation quality...Work experience placement
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