Sr. Director, Regulatory Law, Orthopedics
$178k - $307.05k6149-DePuy Synthes Products Inc. Legal Entity
Sr. Director, Regulatory Law (DePuy Synthes) Location: Raynham, MA; New Brunswick, NJ; West Chester, PA. Key Responsibilities Serve as the senior legal advisor on U.S. and global regulatory law matters affecting medical devices and medical technology across the DePuy Synthes portfolio. Provide strategic legal counsel on regulatory submissions, product clearances and approvals, post‑market surveillance, field actions including recalls, and enforcement actions. Partner with Regulatory Affairs and Quality leadership to interpret and apply FDA, EU MDR/IVDR, and other global regulatory requirements. Serve on Quality Review Boards. Advise on regulatory aspects of product development, clinical investigations, labeling, advertising and promotional activities, including copy review. Advise on commercial activities, including risk of off‑label promotion or activities prior to product clearance or approval. Lead regulatory legal risk assessments and develop mitigation strategies aligned with business objectives. Participate in due diligence for deal activities to assess regulatory compliance or risk associated with transactions. Support global inspections, audits, and interactions with regulatory authorities, including preparation and response strategies. Advise on responses to regulatory bodies with respect to audit findings, including observations or warning letters. Lead or participate in communications with enforcement bodies on a variety of issues. Monitor regulatory developments globally and advise the business on any necessary action or change to policy or procedure. Develop and deploy overarching strategy for interacting with and influencing regulatory policy and collaborate with Government Affairs colleagues. Supervise a paralegal providing support for cross‑functional copy approval. Education & Qualifications Juris Doctor (JD) from an accredited law school (required). Admission to practice law in at least one U.S. jurisdiction (required). Typically requires 12–14 years of progressive legal experience, including significant experience in regulatory law with a private law firm, enforcement body or within a medical device, medical technology, life sciences, healthcare company or another highly regulated industry. Deep knowledge of FDA regulations and global medical device regulatory frameworks (e.g., EU MDR). Global regulatory experience, including collaborating with in‑house or outside counsel internationally. Experience supporting regulatory inspections, enforcement actions or major product remediation activities. Demonstrated experience advising senior leaders on complex regulatory and compliance matters. Proven ability to balance legal risk with business strategy in a fast‑paced environment. Strong communication skills and ability to influence senior executive decision making. Preferred Experience Prior in‑house legal experience supporting a global medical device or medtech organization. Familiarity with regulatory guidelines on digital health, software as a medical device (SaMD), robotics, biologics, combination products or artificial intelligence. Experience supporting mergers, acquisitions or corporate separations in a regulated environment. Strong leadership skills with experience collaborating with colleagues in different legal environments. Additional language skills beyond English. Other Requirements Travel: Up to 15–25% domestic and international. Certifications: None required. Compensation The anticipated base pay range for this position is $178,000.00 – $307,050.00. The position is eligible to participate in the company’s long‑term incentive program. Benefits Vacation – 120 hours per calendar year. Sick time – 40 hours per calendar year (48 hours for employees in Colorado, 56 hours for employees in Washington). Holiday pay, including floating holidays – 13 days per calendar year. Work, Personal and Family Time – up to 40 hours per calendar year. Parental Leave – 480 hours within one year of the birth, adoption or foster care of a child. Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year. Caregiver Leave – 80 hours in a 52‑week rolling period. Volunteer Leave – 32 hours per calendar year. Military Spouse Time‑Off – 80 hours per calendar year. #J-18808-Ljbffr 6149-DePuy Synthes Products Inc. Legal Entity
$178k - $307.05k
...: Legal & ComplianceJob Sub Function: Law Business PartnersJob Category:ProfessionalAll... ...:DePuy Synthes is recruiting for a Sr. Director, Regulatory Law, located in Raynham, MA, New... ...activities of DePuy Synthes across the orthopedic medical device and technology portfolio...SeniorFull timeImmediate start$178k - $307.05k
Sr. Director, Regulatory Law Locations: New Brunswick, New Jersey; Raynham, Massachusetts; West Chester, Pennsylvania. Job Description DePuy Synthes is recruiting for a Sr. Director, Regulatory Law. You will support global regulatory activities in orthopaedics medical...SeniorImmediate start- Johnson & Johnson MedTech is seeking a Sr. Director, Regulatory Law to oversee global regulatory activities in the orthopaedics medical device sector. You will support regulatory strategy, compliance, and innovation through expert legal counsel and collaboration with various...Senior
$178k - $307.05k
...representative bodies, as may be required, regulatory approvals and other customary conditions... ...around the world.Position OverviewSr. Director, Procurement Strategy, Digital and Process... ...characteristics protected by federal, state or local law. We actively seek qualified candidates...SeniorFull timeContract workLocal areaImmediate startFlexible hours$117k - $201.25k
...and recognize their merit.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory... ...and expanding the possibilities of Orthopedics? Ready to join a team that’s reimagining... ...characteristics protected by federal, state or local law. We actively seek qualified candidates...SuggestedFull timeLocal areaImmediate start$122k - $212.75k
...and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should... ...or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans...SeniorFull timeLocal areaImmediate start- Johnson & Johnson is seeking a Sr. Director, Regulatory Affairs for Joints, Digital and Power Tools. Based in multiple eligible locations with travel, you will shape regulatory strategy, lead global submissions, and partner with R&D and platform leaders to accelerate product...Senior
- 6149-DePuy Synthes Products Inc. is looking for a Sr. Director, Regulatory Law to serve as the leading legal advisor on U.S. and global regulatory matters affecting medical devices. The ideal candidate will provide strategic counsel, ensuring compliance with regulatory...
- Johnson & Johnson MedTech is seeking a Senior Regulatory Affairs Manager to lead regulatory strategy for Orthopaedics products across multiple sites in the U.S. You will guide licensing, registrations, and submissions, interfacing with FDA and international agencies to...
$178k - $307.05k
...Function: Legal & ComplianceJob Sub Function: Law Business PartnersJob Category:... ...Description:DePuy Synthes is recruiting for a Sr. Director, Employment Law, located in Raynham, MA... ...bodies, as may be required, regulatory approvals and other customary conditions...SeniorFull timeImmediate start$102k - $177.1k
...talent for Manager, End-to-End Planning-Orthopedics in Raynham, MA and West Chester, PA!ABOUT... ...bodies, as may be required, regulatory approvals, and other customary conditions... ...all applicable federal, state, and local laws/regulations and Corporate DePuy Synthes...Full timeInternshipLocal areaImmediate start- Bausch Health Companies Inc. is seeking a Senior Director of Advertising & Promotion - Regulatory Affairs to lead regulatory reviews for prescription, OTC, and cosmetic products, primarily in the US with Canada support. The role ensures compliance with regulatory agencies...Senior
- ...actively creates it—where your skills and values drive our collective progress and impact. Role Summary The Senior Director of Advertising & Promotion - Regulatory Affairs for drug and device products manages and, if required, participates in the reviews and approvals of...SeniorTemporary workWork at officeFlexible hours
$102k - $177.1k
Manager, End-to-End Planning - Orthopedics (Spine) Location: Raynham, Massachusetts; West Chester, Pennsylvania. Company: Johnson & Johnson... ...product introductions, lifecycle changes, regional launches, regulatory transitions, and supply network changes. Own and manage...$178k - $307.05k
6149-DePuy Synthes Products Inc. Legal Entity seeks a Sr. Director for Global Benefits COE - Orthopedics to lead the organization’s benefits strategy. Responsibilities include overseeing the design of comprehensive benefits programs and ensuring compliance while enhancing...- Cosette Pharmaceuticals, Inc. is seeking a Director of Compliance to lead and continuously improve the company’s enterprise compliance program... ...knowledge of AKS, FCA, PDMA, 340B, Open Payments, and privacy laws, and the ability to steer programs across legal, #J-18808-...Senior
- Johnson & Johnson, DePuy Synthes division, is recruiting a Sr. Director, Regulatory Law, to lead global regulatory activities across orthopedic medical devices. The role is based in Raynham, MA with scope across multiple geographies and entities. The position reports to...
$196k - $342.7k
...recognize their merit.Job Function: Regulatory Affairs GroupJob Sub... ...innovative, and comprehensive orthopedic and neurological business in... ...currently recruiting for a Sr. Director, Regulatory Affairs, Joints,... ...by federal, state, or local law. We actively seek qualified...Full timeLocal areaImmediate start- ...global standards, policies, and governance models aligned with regulatory and internal requirements. Drive continuous improvement... ...Sigma, or Operational Excellence deployment. Prior experience in orthopedic, medical device, or highly regulated manufacturing environments...Senior
- Regulatory Affairs Program Manager (Medical Device Divestiture) Location: Raynham, MA / West Chester, PA / Palm Beach Gardens, FL (Hybrid 3-4 days onsite) Duration: 12+ Months (Extension Possible) Overview We are seeking an experienced Regulatory Affairs Program Manager...
$228.41k - $247.15k
Basic Qualifications Education: Bachelor’s degree or equivalent is required plus a minimum of 15 years of demonstrated leadership; or Master's degree plus a minimum of 13 years of demonstrated leadership. years of demonstrated leadership; or Master's degree plus a minimum...Remote workFlexible hours$178k - $307.05k
...representative bodies, as may be required, regulatory approvals and other customary... ...the world.Position SummaryThe Sr. Director, Global Benefits COE - Orthopedics provides enterprise‑level leadership... ...by federal, state or local law. We actively seek qualified candidates...SeniorFull timeLocal areaImmediate start$178k - $307.05k
...representative bodies, as may be required, regulatory approvals and other customary conditions... ...around the world.Job OverviewThe Sr. Director, Security & Defense is a senior technology... ...characteristics protected by federal, state or local law. We actively seek qualified candidates...SeniorFull timeLocal areaImmediate start$128k - $160k
## Sr. Materials Planning ManagerApplyremote type: Hybrid Workinglocations: Lakeville, MAtime type: Full timeposted on: Posted 3 Days... ...employment or continued employment. Any employer who violates this law shall be subject to criminal penalties and civil liability.* #J-1...SeniorContract workTemporary workWork experience placementRemote workMonday to FridayFlexible hours$137k - $235.75k
...Synthes is recruiting for a(n) Sr. Manager, TPO R&D Labs .... ...announced plans to separate our Orthopedics business to establish a standalone... ...bodies, as may be required, regulatory approvals and other customary... ...protected by federal, state or local law. We actively seek qualified...SeniorFull timeLocal area$122k - $212.75k
...Description:DePuy Synthes is recruiting for a(n) Sr. Manager, Portfolio Project Management,... ...Johnson announced plans to separate our Orthopedics business to establish a standalone... ...bodies, as may be required, regulatory approvals and other customary conditions...SeniorFull timeImmediate start$178k - $307.05k
...representative bodies, as may be required, regulatory approvals and other customary conditions... ...$2.2 B in annual spend. The Sr. Director will build the team, develop the vision,... ...characteristics protected by federal, state or local law. We actively seek qualified candidates...SeniorFull timeLocal areaImmediate start$178k - $307.05k
...DePuy Synthes is recruiting for a Sr. Director, Learning, Performance, and Inclusion- Orthopedics, located in Raynham, MA, West... ...bodies, as may be required, regulatory approvals and other customary conditions... ...by federal, state or local law. We actively seek qualified...SeniorFull timeContract workLocal areaImmediate start$122k - $212.75k
...Synthes is recruiting for a(n) Sr. Manager, Procurement R&D... ...announced plans to separate our Orthopedics business to establish a standalone... ...bodies, as may be required, regulatory approvals and other customary... ...protected by federal, state or local law. We actively seek qualified...SeniorFull timeContract workWork experience placementLocal areaImmediate start$178k - $307.05k
...representative bodies, as may be required, regulatory approvals and other customary conditions... ...consultation processes.Job OverviewThe Sr. Director, IT Portfolio Management is a senior... ...characteristics protected by federal, state or local law. We actively seek qualified candidates...SeniorFull timeWork at officeLocal areaImmediate start
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