Director, Regulatory Affairs
$174k - $246kEdwards Lifesciences Belgium
Make a meaningful difference to patients around the world! Our Legal team works to protect our patients, team members, and innovations with the utmost diligence and care. You'll have the opportunity to work with a dedicated team and build lasting partnerships with stakeholders across our global organization. Your legal knowledge and contributions will help us ensure that we are supporting the needs and interests of the patients we serve. The Director, Regulatory Counsel reports to the Vice President, Regulatory Counsel and will be responsible for timely review and approval of advertising and promotion materials, provision of advice and counsel with respect to fraud and abuse issues, analysis of clinical contracts, assistance with state licensing, support for sales contracting, and other legal regulatory duties as needed. The Director, Regulatory Counsel will closely partner with Marketing, Clinical Affairs, Regulatory Affairs, Compliance and other functional groups within Edwards, and will require a thorough understanding of each of Edwards' business units and the products they manufacture and sell. The successful candidate will have a unique opportunity to help Edwards achieve its business objectives by providing practical, timely and effective legal counsel, while minimizing potential legal risks (and having fun doing it as part of a great team). Work Schedule: Given the collaborative and complex nature of this work, this role is in person full time in Irvine, California. How you'll make an impact: Providing legal guidance to Edwards, including working closely with each of the business units and Corporate functions. Reviewing and advising on a variety of advertising and promotional pieces, including print and digital ads, social media campaigns, speaker presentations, and other materials to determine compliance with applicable regulations and policies and assess corporate risk. Providing advice and counsel with respect to fraud and abuse issues. Reviewing and advising on clinical contracts and a variety of legal issues related to clinical trials. Reviewing, negotiating, and advising on strategic clinical and commercial contracts across business units Developing and harmonizing standard processes and templates; creating, improving, and institutionalizing knowledge base for the Healthcare Regulatory team. Developing and delivering legal education to business colleagues in specific areas (e.g., regulatory approval processes, pathways to market (510(k), PMA, etc.), requirements for FDA-regulated clinical investigations, etc.). Monitoring legal developments applicable to the Healthcare Regulatory and medical device spaces and developing expertise in strategic focus areas. Other duties and responsibilities as assigned. What you'll need (Required): Juris Doctor from ABA-accredited law school with 8 years of legal experience at a law firm or in-house legal department. Strong written and verbal communication and interpersonal skills, including the ability to convey nuanced legal concepts/issues clearly and succinctly to legal and business decision makers. Excellent independent problem-solving, critical thinking, and investigative skills Strategic thinking, proactive mindset, and excellent problem-solving abilities. Ability to be a team player and a trusted business partner. Ability to work under pressure and prioritize projects and tasks appropriately. What else we look for (Preferred): Background in life sciences, MedTech, pharmaceuticals, or related healthcare industry experience preferred. Experience in advertising and promotion in the medical device or pharmaceutical industry or at a healthcare system. Experience providing advice and counsel with respect to fraud and abuse issues in the medical device or pharmaceutical industry. Prior-in house experience in life sciences, MedTech, pharmaceuticals, or related healthcare industry preferred. Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families. For California (CA), the base pay range for this position is $174,000 to $246,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities. #J-18808-Ljbffr
$226.5k - $317.1k
About the RoleThe Senior Director Regulatory Affairs Strategy will play a key role in guiding assigned projects throughout development and lifecycle management by providing regulatory thought leadership and leveraging their extensive development experience. The individual...SuggestedWork at officeLocal areaRemote work- ...Sr. Manager / Director, Regulatory Affairs Relocation Required to Southern CA Role Overview We are seeking an experienced regulatory affairs leader to drive strategy, oversee submissions, and guide interactions with global health authorities. This individual will play...SuggestedRelocation
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- Job-ID31508263Reference25-04457 Responsibilities: In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets...SuggestedWork at office
$175k - $230k
Overview Director, Public Sector Consulting - Regulatory Compliance & GrantsLocations: Chicago, IL | Irvine, CA | San Francisco Bay Area, CA (Hybrid)Remote... ...in Public Administration, Public Policy, Public Affairs, Accounting or related field; Master’s degree preferred...Full timeLocal areaRemote workFlexible hours$173k - $245k
...discovering lasting solutions for unmet patient needs. Our Senior Director, Global Compliance Policy and Program is a unique career... ...optimization efforts that strengthen operational excellence and regulatory adherence. Oversight and management of government inquiries related...Full timeWork experience placementLocal area- ...Reference26-00132 Responsibilities: Support the Senior Director in developing and executing regional regulatory strategies for QOL initiatives within specific... ...preferred. 5+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with...
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$66.1k - $118.3k
...able to communicate research and data findings in a meaningful way. You will be responsible for monitoring internal and external regulatory audits. And you will be expected to monitor changes in requirements to mitigate risks and achieve compliance. You’ll enjoy the flexibility...Work experience placementLocal areaRemote work$99.7k - $152.08k
The Sr. Export Compliance Specialist supports the company’s export compliance program to ensure compliance with U.S. export control regulations and protect sensitive technology and information. This role partners cross-functionally to provide practical compliance guidance...Permanent employmentFull timeFor contractorsCasual workWork at office- ...medical technology or similar. 5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the... ...verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
$92k - $148.35k
...individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Irvine, California, United States...Full timeContract workTemporary workLocal areaImmediate startFlexible hours3 days per week- ...Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S... ...of international product registrations and related regulatory affairs activities, including execution of procedures and systems...Work at office
$85k - $130k
Job SummarySr Regulatory Affairs Specialist is an accomplished regulatory professional with a successful work history with leading regulatory initiatives and partnering with Sales and Marketing teams in obtaining domestic and internal regulatory clearances for Masimo products...Work experience placementLocal areaWorldwideFlexible hours- Company DescriptionAt the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight...
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$114.91k - $141.95k
...'ll do:As a Compliance Assistant Manager you'll be a subject matter expert and provide advice, oversight and guidance related to regulatory compliance risks, control effectiveness, root cause analysis, and issue review and validation. You'll provide leadership and direction...Full timeContract work$86k - $114k
...to the United States and its allies. Operating in a fast-growing, high-impact environment, we take creative ownership of complex regulatory matters to build and manage efficient, top-tier compliance processes. We are deeply passionate about the law and policy of defense...Full timeFor contractorsWork experience placementImmediate start- ...Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market... ...communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial....Full timeLocal area
$145.48k - $183.51k
Consulting Director, Regulatory Analyst (Utilities/Power/Renewables)Are you ready to lead transformative environmental projects that power communities and drive sustainable innovation? ERM is seeking a visionary Consulting Director, Power, Energy & Regulatory Advisory...Full timeContract workFixed term contractCasual workWorldwideFlexible hours- ...Description: MFG is seeking a detail‑oriented Compliance Manager to join our firm. In this position, you will perform a variety of regulatory compliance and risk management duties. Additional responsibilities may include credit monitoring, financial analysis & reporting,...Local area
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- Anduril is looking for a highly motivated individual to join our Test and Evaluation Safety and Standards team in Costa Mesa, California. This role involves ensuring compliance with DCMA 8210 regulations while developing safety management systems and operational standards...
$97k - $189k
...matter and are part of something important, ensuring the abilities of all employees are used to their fullest potential. The Managing Director Strategic Claim Oversight leads the Severity & Excess Accounts team that both directly handles and oversees the highest exposure...Full timeWork experience placementWork at office- Job Summary:The Assurance Director title is reserved for professionals who achieve recognition in a technical area of assurance and risk management. The person is qualified to perform certain limited yet critical additional technical functions as an Engagement Director...Work at office
$110.1k - $183.4k
Work Flexibility: Hybrid or OnsiteStaff International Regulatory Affairs SpecialistIrvine, CAIn this International Regulatory Affairs role, you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways. This is a meaningful...Full timeFor contractorsLocal area
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