Role Description We are seeking a Compliance & Corporate Governance Advisor to support the Drilling Services division in Salt Lake City, UT. This role supports core compliance workflows, including: - Hotline intake - Investigations support - Policy management - Training tracking - Monitoring - Third-party due diligence The position reports directly to the General Counsel – Drilling Services and works closely with regional management, HR, Finance, and operations. The role is well suited for a detail-oriented compliance, legal, or risk professional who can: - Spot issues - Follow through on key workflows - Manage documentation carefully - Contribute across a lean legal team ESG/ESH responsibilities are separately managed but require coordinated interaction. Qualifications - Bachelor’s degree required - Advanced degree in business, law, or a related field preferred - Professional certifications such as CCEP, CCEP-I, CRCM, or similar are a plus Requirements - Minimum 5 years of experience in compliance, risk management, legal support, legal operations, corporate governance, or related operational roles - Experience in industrial services, energy, mining, manufacturing, or similarly complex environments is preferred - Working knowledge of compliance program elements, including ABC frameworks, hotline processes, investigations support, and third-party risk management - Experience in, or strong interest in, working in a corporate legal department, including governance support such as entity management, filings, board materials, or related work; public company experience is a plus - Excellent written and verbal English communication skills - Proactive, solutions-oriented mindset with sound judgment and an ability to spot issues and help resolve them - Excellent organizational skills, strong attention to detail, and ability to manage multiple projects, filings, and deadlines - Ability to work independently, learn new subject matter quickly, and contribute flexibly across a lean legal team Benefits - A strong compensation plan - Medical, vision, and dental program - Retirement program - Employee recognition rewards program (BRAVO) - Employee assistance program

Role Description Our Compliance team blends regulatory expertise with data-driven thinking to make sure our products meet legal and policy requirements and deliver real value to customers. In a fast-moving, digital environment, they stay one step ahead by finding smart, scalable ways to manage conduct risk. We're looking for a Regulatory Compliance Manager to keep our consumer protection practice in compliance. You'll advise on investment compliance (MiFID II, UCITS, MAR) and support with establishing and monitoring related controls. What you'll be doing: - Acting as a regulatory compliance expert regarding client onboarding, product governance, and investment product launches - Monitoring, testing, and reporting on the effectiveness of our regulatory architecture - Drafting, implementing, and rolling out compliance plans, frameworks, and policies - Participating and advising on product launches, providing expert regulatory advice to support the Operations team to fully comply with local regulations - Developing and executing a world-class compliance framework and training programme - Supporting interactions with regulators Qualifications - Practical knowledge of MiFID II, UCITS, and MAR - Experience in compliance risk management within a consultancy, compliance function, or regulator - The ability to work well under pressure, manage multiple projects at once, and meet tight deadlines - Knowledge of how to conduct regulatory gap analysis - Familiarity with policy creation and implementation - A solid understanding of the interplay between compliance risk and business risk - The ability to communicate positively with regulators and members of various internal teams - Multitasking skills with impeccable attention to detail - Excellent analytical, communication, and interpersonal skills Important Notice for Candidates - Only apply through official Revolut channels. - We don't use any third-party services or platforms for our recruitment. - Always double-check the emails you receive. - Make sure all communications are being done through official Revolut emails, with an @revolut.com domain. - We won't ask for payment or personal financial information during the hiring process. - If anyone does ask you for this, it's a scam. Report it immediately.

Role Description Seeking someone passionate about information security and customer service to assist customers in meeting their cybersecurity regulatory and legal requirements. Analysts will work with customers to: - Develop formalized information security policies - Analyze the efficacy of current policies and procedures - Evaluate the risks posed by third-party providers - Provide security awareness training to clients - Provide insight into cybersecurity regulations Analysts also lend their expertise to internal initiatives related to cybersecurity governance and compliance. Qualifications - 1-3 years’ experience in an IT, Cybersecurity, or GRC-related field (Preferred) - Preferred certifications: CompTIA Security+, ISC2 CC, OCEG GRCP - Knowledge of Secure Software Development Life Cycle (SSDLC) practices is a plus - Basic operational capabilities for the Office 365 stack (Microsoft Word, Excel, Outlook) - Strong ability to direct self-work with excellent organizational and time management skills - Excellent verbal and written communication skills, especially when communicating technical concepts to non-technical audiences - Critical and creative thinking to strategize how to add value to customer engagements and improve processes - Exceptional spelling and grammar skills for writing and proofreading documents - Ability to remain flexible as processes continuously improve Requirements - Should be willing to accept a long-term work-from-home arrangement - Should be amenable to a permanent night shift schedule

Role Description EssilorLuxottica 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 hands-on, execution-focused contractor position responsible for: - Reviewing technical documentation to ensure regulatory compliance. - Authoring submission materials. - Supporting documentation regulatory strategies across US, EU, and global markets. - Working cross-functionally with R&D, clinical, project management, and quality teams. 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, and cybersecurity. - Strong working knowledge of FDA regulations (21 Parts 807, 820) and guidance documents. - Experience with Canadian regulations and EU MDR (2017/745) including Class IIa, Tech docs Annex II/III. - Demonstrated ability to work independently as a contractor in a fast-paced environment. Requirements - Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable). - Perform detailed regulatory gap assessments against 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 and Substantive Review coordination. - Draft and submit responses to FDA requests for Additional Information. - Update submission content and modules as required. - Interface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process. - Provide regulatory leadership through FDA clearance. - Conduct EU MDR readiness assessment aligned with Notified Body expectations. - Perform critical review and gap analysis of EU MDR technical file. - Lead or support submission to obtain CE Mark. - Perform regulatory strategy and classification confirmation for Health Canada submissions. - Develop and maintain a harmonized global regulatory dossier. - Define and implement documentation reuse strategies across justification. - Author a comprehensive global strategy document outlining pathways, timelines, and key risks. - Provide ongoing regulatory guidance and advisory support to cross-functional teams. - Lead or support global regulatory submissions as needed. Benefits - Type: Contractor (Hourly, Time and Materials). - Expected duration: 6-12 months (depending on FDA review timelines). - Start: Immediate. - Workload: Flexible estimate 20-40 hours per week. - Location: Remote.