Hire the Best Regulatory Compliance Freelancers in New York

I’m a New York–licensed attorney with 5+ years of in-house legal experience supporting fast-paced fintech and tech companies. I specialize in drafting, reviewing, redlining, and simplifying commercial contracts, privacy policies, and terms of use so founders, operators, and lean teams can move quickly with confidence and clarity. I’ve reviewed 500+ agreements across a range of business functions and frequently draft user-friendly Terms & Conditions for marketing and promotional campaigns, Privacy Policies, and Terms of Use, balancing compliance with clarity to avoid confusing customers or triggering legal risk. Contract Types I Work With: • NDAs, MSAs, SaaS, Licensing & Partnership Agreements, SOWs, Lead Generation, and more • Employment & Contractor Agreements • Promotional Terms & Conditions (with compliant disclaimers) Services I Offer: • Contract redlines with plain-language explanations • Deal risk spotting, negotiation levers, and structure feedback • Compliance checklists and process optimization • Privacy Policy and Terms of Use drafting and reviewing • Fast turnaround available (24hr rush supported) Note: I provide contract consulting and legal drafting, not formal legal representation. I am licensed in New York. Let’s make your contracts, polices, and terms work for your business, clearly, efficiently, and with minimal friction.

𝐍𝐞𝐞𝐝 𝐭𝐨 𝐟𝐢𝐥𝐥 𝐤𝐞𝐲 𝐫𝐨𝐥𝐞𝐬 𝐰𝐢𝐭𝐡 𝐭𝐨𝐩-𝐭𝐢𝐞𝐫 𝐭𝐚𝐥𝐞𝐧𝐭? That’s where I come in. I specialize in identifying, engaging, and delivering the right professionals - fast. For the past 18 years, I’ve focused exclusively on recruiting—helping employers connect with qualified professionals who make excellent hires. My track record of success has resulted in a 5-star Upwork rating (Top 10% Upwork Freelancer) and consistent praise from clients and employers alike. 𝐐𝐮𝐢𝐜𝐤 𝐈𝐧𝐭𝐫𝐨𝐝𝐮𝐜𝐭𝐢𝐨𝐧: 🔹Top Rated Plus/Top 10% Upwork freelancer with all 5-star reviews ⭐⭐⭐⭐⭐ 🔹US Citizen based in New York State 🔹18 years of full-cycle recruitment experience in both aggressive outbound recruitment (agency) and strategic talent partner (corporate) capacities 𝐂𝐨𝐧𝐬𝐮𝐥𝐭𝐢𝐧𝐠 𝐅𝐨𝐜𝐮𝐬 𝐀𝐫𝐞𝐚𝐬: (a la carte or full-service) 🔸Full-cycle Recruitment – strategizing with hiring manager ➙ sourcing ➙ screening ➙ candidate presentation to hiring manager ➙ interview coordination with hiring team ➙ offer presentation 🔸Recruitment Process – Audit current tools and sourcing platforms, review interview process and propose ways of improvement 🔸Recruitment Strategy Development – Discover needs, define ideal profile, sourcing/outreach, selection/interview framework, metrics/improvement 🔸Job Description Creation & Optimization – Write or refine postings to attract stronger candidates 🔸Candidate Experience Optimization – Review application-to-hire process and identify/reduce friction points that deter talent. 🔸Recruiter Training – modern sourcing techniques, proper ways to approach and sell opportunities 🔸Hiring Manager Interview Training – effective interview format and questions to assess talent 𝐌𝐨𝐬𝐭 𝐑𝐞𝐜𝐞𝐧𝐭 𝐔𝐩𝐰𝐨𝐫𝐤 𝐄𝐧𝐠𝐚𝐠𝐞𝐦𝐞𝐧𝐭: Contract Recruiter for a health tech SaaS start-up, fully embedded as an internal team member with company email, employee profile, full system access, and direct collaboration with hiring managers and interview teams. • Directed end-to-end recruitment strategy in a fast-paced, high-growth environment • Managed full-cycle hiring for revenue-driving sales, key marketing, IT/engineering (Principal Architect, Sr. Software Engineer), and HR leadership roles • Proactively sourced top talent using LinkedIn Recruiter and other platforms • Oversaw applicant flow through Rippling ATS, ensuring smooth candidate experience and data accuracy • Conducted high-volume candidate screening (phone/video) and coordinated interview logistics with hiring teams • Partnered with C-suite and VP-level leaders to provide weekly hiring updates, manage interview processes, and deliver feedback loops • Quickly mastered internal processes and technology platforms to streamline recruitment operations ⭐𝐓𝐞𝐬𝐭𝐢𝐦𝐨𝐧𝐢𝐚𝐥𝐬⭐ "𝑆𝑒𝑎𝑛 ℎ𝑎𝑠 𝑏𝑒𝑒𝑛 𝑎𝑛 𝑖𝑛𝑣𝑎𝑙𝑢𝑎𝑏𝑙𝑒 𝑟𝑒𝑐𝑟𝑢𝑖𝑡𝑚𝑒𝑛𝑡 𝑝𝑎𝑟𝑡𝑛𝑒𝑟 𝑤ℎ𝑜 𝑖𝑠 𝑑𝑒𝑑𝑖𝑐𝑎𝑡𝑒𝑑 𝑡𝑜 𝑒𝑣𝑒𝑟𝑦 𝑠𝑒𝑎𝑟𝑐ℎ 𝑎𝑛𝑑 𝑐𝑜𝑚𝑚𝑖𝑡𝑡𝑒𝑑 𝑡𝑜 𝑎 𝑠𝑢𝑐𝑐𝑒𝑠𝑠𝑓𝑢𝑙 𝑜𝑢𝑡𝑐𝑜𝑚𝑒. 𝐼 𝑠𝑡𝑟𝑜𝑛𝑔𝑙𝑦 𝑟𝑒𝑐𝑜𝑚𝑚𝑒𝑛𝑑 𝑟𝑒𝑎𝑐ℎ𝑖𝑛𝑔 𝑜𝑢𝑡 𝑡𝑜 𝑆𝑒𝑎𝑛 𝑖𝑓 𝑦𝑜𝑢 𝑛𝑒𝑒𝑑 𝑎𝑑𝑑𝑖𝑡𝑖𝑜𝑛𝑎𝑙 𝑟𝑒𝑐𝑟𝑢𝑖𝑡𝑚𝑒𝑛𝑡 𝑝𝑜𝑤𝑒𝑟." - 𝑀𝑎𝑟𝑦𝑎𝑛𝑛 𝐾. (𝐶ℎ𝑖𝑒𝑓 𝐻𝑢𝑚𝑎𝑛 𝑅𝑒𝑠𝑜𝑢𝑟𝑐𝑒𝑠 𝑂𝑓𝑓𝑖𝑐𝑒𝑟) "𝑆𝑒𝑎𝑛 𝑤𝑎𝑠 𝑎𝑤𝑒𝑠𝑜𝑚𝑒 𝑡𝑜 𝑤𝑜𝑟𝑘 𝑤𝑖𝑡ℎ. 𝑃𝑟𝑜𝑓𝑒𝑠𝑠𝑖𝑜𝑛𝑎𝑙, 𝑒𝑓𝑓𝑖𝑐𝑖𝑒𝑛𝑡, 𝑎𝑛𝑑 𝑚𝑎𝑑𝑒 𝑡ℎ𝑒 𝑝𝑟𝑜𝑐𝑒𝑠𝑠 𝑠𝑚𝑜𝑜𝑡ℎ 𝑓𝑟𝑜𝑚 𝑠𝑡𝑎𝑟𝑡 𝑡𝑜 𝑓𝑖𝑛𝑖𝑠ℎ. 𝐻𝑖𝑔ℎ𝑙𝑦 𝑟𝑒𝑐𝑜𝑚𝑚𝑒𝑛𝑑!" – 𝐶𝑎𝑟𝑜𝑙 𝑅. (𝐷𝑖𝑟𝑒𝑐𝑡𝑜𝑟 𝑜𝑓 𝑅𝑒𝑐𝑟𝑢𝑖𝑡𝑚𝑒𝑛𝑡) "𝐼 ℎ𝑎𝑣𝑒 𝑤𝑜𝑟𝑘𝑒𝑑 𝑤𝑖𝑡ℎ 𝑆𝑒𝑎𝑛 𝑏𝑜𝑡ℎ 𝑎𝑠 𝑎 𝑐𝑎𝑛𝑑𝑖𝑑𝑎𝑡𝑒 𝑎𝑛𝑑 𝑎 𝑐𝑙𝑖𝑒𝑛𝑡. 𝑆𝑒𝑎𝑛 𝑖𝑠 𝑝𝑟𝑜𝑓𝑒𝑠𝑠𝑖𝑜𝑛𝑎𝑙, ℎ𝑖𝑔ℎ𝑙𝑦 𝑘𝑛𝑜𝑤𝑙𝑒𝑑𝑔𝑒𝑎𝑏𝑙𝑒 𝑎𝑛𝑑 𝑤𝑖𝑑𝑒𝑙𝑦 𝑐𝑜𝑛𝑛𝑒𝑐𝑡𝑒𝑑 𝑤𝑖𝑡ℎ 𝑣𝑎𝑟𝑖𝑜𝑢𝑠 𝑐𝑎𝑛𝑑𝑖𝑑𝑎𝑡𝑒𝑠." – 𝐶ℎ𝑎𝑟𝑙𝑒𝑠 𝐿. (𝑉𝑖𝑐𝑒 𝑃𝑟𝑒𝑠𝑖𝑑𝑒𝑛𝑡) 𝐑𝐞𝐜𝐫𝐮𝐢𝐭𝐦𝐞𝐧𝐭 𝐓𝐨𝐨𝐥 𝐏𝐫𝐨𝐟𝐢𝐜𝐢𝐞𝐧𝐜𝐢𝐞𝐬: 🔹Big Biller Applicant Tracking System (ATS/CRM) 🔹Rippling (ATS) 🔹Ashby (ATS) 🔹LinkedIn Recruiter (Candidate sourcing) 🔹Sales Navigator (Candidate sourcing) 🔹Indeed (Candidate sourcing) 🔹CareerBuilder (Candidate sourcing) 🔹Dux-Soup Turbo (LinkedIn outreach) 🔹SignalHire (Contact Data) 🔹Hunter (Contact Data) 🔹Woodpecker (Email outreach) 🔹Bouncer (Email verification) 🔹Slack 𝐂𝐞𝐫𝐭𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬: ✔ AIRS Certified Diversity Recruiter ✔ AIRS Professional Recruiter Certification 𝐀𝐯𝐚𝐢𝐥𝐚𝐛𝐢𝐥𝐢𝐭𝐲: Flexible, but generally available on a project/search or hourly basis. 𝑃𝑙𝑒𝑎𝑠𝑒 𝑓𝑒𝑒𝑙 𝑓𝑟𝑒𝑒 𝑡𝑜 𝑟𝑒𝑎𝑐ℎ 𝑜𝑢𝑡 𝑤𝑖𝑡ℎ 𝑎𝑛𝑦 𝑞𝑢𝑒𝑠𝑡𝑖𝑜𝑛𝑠 𝑎𝑏𝑜𝑢𝑡 𝑚𝑦 𝑠𝑒𝑟𝑣𝑖𝑐𝑒 𝑜𝑟 𝑎𝑣𝑎𝑖𝑙𝑎𝑏𝑖𝑙𝑖𝑡𝑦. 𝑇ℎ𝑎𝑛𝑘 𝑦𝑜𝑢!

I am a skilled and experienced biomedical engineer specializing in the design and development of medical devices/medical technologies. I have worked in the medical technology industry for over a decade and have a Bachelors of Engineering and Masters of Science in biomedical engineering. With extensive expertise in design quality, quality assurance, and regulatory affairs within the industry, I am well-equipped to handle any challenges that may arise. Throughout my career, I have successfully worked with both large medical device corporations and startups, gaining invaluable insights into the FDA submission process and the specific requirements based on technology risk. I possess a thorough understanding of how to navigate the complex regulatory landscape and bring medical devices through the approval process. My previous accomplishments include the development and maintenance of robust quality systems, leading design quality projects for Class II/III medical devices by employing risk analysis and design control strategies. Additionally, I have extensive experience in interacting with the FDA throughout the pre-submission and 510(k)/PMA/De Novo submission processes, ensuring compliance and smooth communication. Furthermore, I am well-versed in auditing quality systems based on 21 CFR 820 and ISO 13485. This ensures that my clients can confidently rely on my expertise to meet and exceed regulatory requirements and industry best practices. If you are in need of a highly skilled MedTech consultant with a proven track record and in-depth knowledge of the medical technology industry, I am confident that my qualifications make me the ideal candidate for your project. Let's collaborate to bring your ideas to life and transform healthcare for the better.

With an extensive background in FDA regulations and compliance, I am a seasoned professional dedicated to ensuring top-notch standards in FDA regulatory affairs. I have a proven track record of collaborating effectively with the FDA, ensuring compliance, and swiftly implementing corrective actions during inspections. My commitment to transparency and excellence has fortified my reputation as a reliable specialist in regulatory compliance and project management. In addition to my regulatory expertise, I bring a wealth of experience in translating complex legal and technical documents, drafting precise legal materials, and designing FDA-compliant labels. My analytical and problem-solving skills, coupled with a passion for continuous improvement, make me a valuable asset to any organization striving for excellence in compliance and safety.

Clinical laboratories don’t fail because of analyzers—they fail at the intersection of systems, data integrity, and workflow. I help laboratories and diagnostic organizations resolve complex issues in: -LIMS and analyzer integration -QC drift and data integrity risks -validation and audit readiness (GxP, FDA, ISO) -system governance across regulated environments With 15+ years across clinical labs, diagnostics manufacturing, and laboratory systems, I bring both hands-on and strategic expertise—bridging the gap between laboratory operations, IT, and quality. If you're dealing with a complex lab/system issue and need experienced insight—not guesswork—I can help.

Expert-level Regulatory & Process Technical Writer and editor with over 20 years experience, including FDA-regulatory Quality documentation. Highlights: - Draft press release and technical content for advertising and marketing agency clients using SEO methods for Google Search & Apple Search Ads (certified) on AWS and EV topics. - Author 510k submission for NY Medicaid provider and trained/guided staff on QMS management, which included authoring a collection of FDA quality processes and policy. - Draft Teacher’s Notes for Senior Researcher at UVA Darden Graduate School using Standard Harvard Methodology. - Architect knowledgebase wiki using Bookstack for production company. - Wordpress design and web editing / maintenance for independent pharmacy owner clients. - Spearhead HIPAA-compliant Disaster Recovery plan creation for insurance organization. - Prepare drafts for Deloitte Tax clients of submission to IRS for tax incentive program. - Customized Mozilla’s Bugzilla template toolkit to architect an enterprise-scale application; validated for regulatory use; led training sessions via webinars and in-person training sessions for each group based on custom roles and permissions. Recieved award for co-spearheading the design of a brand standards resource; acted as company-wide style czar for all client-facing documentation.