MedTech Regulatory Specialist - Global Submissions
Vita Global Sciences, a Kelly Company
Kelly Science and Clinical FSP is seeking a Regulatory Specialist for a long-term engagement with a Global MedTech client. The role is full-time with benefits and is part of our FSP division, a managed solution within Kelly Services, Inc. Responsibilities include providing independent regulatory guidance, leading licenses and registrations, ensuring compliance, preparing and submitting regulatory documents, and supporting audits. Collaboration across product development teams is essential. #J-18808-Ljbffr Vita Global Sciences, a Kelly Company
- ...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.... ...legal experience, you will advise on regulatory submissions, monitor changes in law, and collaborate with...Suggested
- 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...Suggested
- ...Science and Clinical FSP is currently seeking a Regulatory Specialist for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP... ...: provides assistance in preparation and submission of global regulatory documents. Position...SuggestedFull time
- 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...Suggested
- Johnson & Johnson MedTech is seeking a Senior Regulatory Affairs Manager to lead regulatory strategy for Orthopaedics products across multiple sites... ...the U.S. You will guide licensing, registrations, and submissions, interfacing with FDA and international agencies to...Suggested
- ...partnering with regional finance teams and external banks to drive process improvements and global treasury excellence. The role emphasizes cross-functional collaboration, adherence to internal controls, and exposure to Kyriba, with #J-18808-Ljbffr Johnson & Johnson MedTech
$178k - $307.05k
...expertise in Innovative Medicine and MedTech, we are uniquely positioned... ...for a Sr. Director, Regulatory Law, located in Raynham, MA,... ...legal leader supporting the global regulatory activities of DePuy... ...legal counsel on regulatory submissions, product clearances and approvals...Full timeImmediate start- ...recruiting an Export Controls Analyst to support DePuy Synthes' global trade compliance program. The role covers export... ...legal, quality, and IT teams. A Bachelor’s degree and 5+ years in export controls are required. #J-18808-Ljbffr Johnson & Johnson MedTech
- Regulatory Affairs Manager / Regulatory Affairs Specialist role Established in 1991, Collabera has been a leader in IT staffing... ...through Staff Augmentation, Global Talent Management, Value Added Services... ...the preparation, analysis, and submissions dossiers to various governing...Permanent employmentLocal area
- ...Development to be based in Raynham, MA, with responsibilities spanning regulatory readiness and development of regulatory solutions. You will... ...of PM experience in regulated environments are required; PM certification is a plus. #J-18808-Ljbffr Johnson & Johnson MedTech
$178k - $307.05k
Sr. Director, Regulatory Law (DePuy Synthes) Location: Raynham, MA; New... ...legal advisor on U.S. and global regulatory law matters affecting... ...legal counsel on regulatory submissions, product clearances and... ...supporting a global medical device or medtech organization. Familiarity...Immediate start$178k - $307.05k
Sr. Director, Regulatory Law Locations: New Brunswick, New Jersey; Raynham... ...Law. You will support global regulatory activities in orthopaedics... ...legal counsel on regulatory submissions, product clearances,... ...supporting a global medical device or medtech organization. Familiarity...Immediate start- Johnson & Johnson, a global leader in health care, is recruiting a Quality/Compliance Analyst - Customer Service. The role focuses on... ...across functions to standardize practices and improve efficiency in a regulated environment. #J-18808-Ljbffr Johnson & Johnson MedTech
$109k - $174.8k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...representative bodies, as may be required, regulatory approvals and other customary conditions... ...the development and maintenance of global harmonized processes and procedures for...Full timeLocal area- Amneal is seeking an Associate Director of PV Compliance to lead the Global Patient Safety (GPS) compliance and quality management program, ensuring adherence to global PV regulations and company procedures. You will supervise audits, inspections, SDEA lifecycle management...
- DePuy Synthes is seeking a MedTech Sales professional to cover the Charlottesville VA territory, including Richmond, VA. You will promote orthopaedic solutions to surgeons, hospitals, and healthcare systems while building clinicians and KOL relationships to drive adoption...
$175.5k
...expertise in Innovative Medicine and MedTech, we are uniquely positioned... ...be considered as a single submission. The Manager, Reporting &... ...impact in a complex, global organization. - Strong experience... ...bodies, as may be required, regulatory approvals and other customary...Full timeLocal areaImmediate start- Regulatory Affairs Program Manager (Medical Device Divestiture) Location: Raynham, MA / West Chester, PA / Palm Beach... ...Divestiture initiative. This role will manage the transfer of global regulatory registrations, submissions, and documentation from a large healthcare...
- ...Synthes, part of Johnson & Johnson, is seeking a Project Manager, Business Product & Development, to lead regulatory business product initiatives in a regulated MedTech environment. You will collaborate with Regulatory Affairs, Quality, IT, and business teams to deliver...
$117k - $201.25k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...recognize their merit. Job Function Regulatory Affairs Group Job Sub Function Regulatory... ...planning, pre-marketing, and related submissions to support optimal timelines for new/modified...Local areaImmediate start- ...needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (... ...savings plan, Life Insurance, Disability Insurance. Job Description Regulatory affairs with Technical Files, or equivalent in an R&D or quality...Permanent employment
$122k - $212.75k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...representative bodies, as may be required, regulatory approvals and other customary conditions... ...capabilities. Preferred: Experience in global or multi‑site supply chain operations....Full timeImmediate start$178k - $307.05k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...representative bodies, as may be required, regulatory approvals and other customary conditions... ....About DePuy SynthesDePuy Synthes is a global leader in orthopaedics, advancing...Full timeLocal areaImmediate startWorldwide- Collegium Pharmaceutical, Inc. is seeking a Manager of Regulatory Affairs to lead regulatory support for marketed products and development... ...with applicable regulations. The position focuses on IND/NDA submissions, regulatory publishing, and labeling management, with a...
$122k - $245k
...expertise in Innovative Medicine and MedTech, we are uniquely positioned to... ...be considered as a single submission. The Sr. Manager, Finance Master Operations is a global role within the Supply Chain... ...support audit readiness and regulatory requirements. - Lead, mentor...Full timeLocal areaImmediate start- ...President of the Trauma Business Unit. The Executive Administrative Assistant provides high‑level administrative, coordination, and operational support to the President and leadership ecosystem, enabling efficiency and executive focus. #J-18808-Ljbffr Johnson & Johnson MedTech
$94k - $151.8k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...representative bodies, as may be required, regulatory approvals and other customary conditions... ...analytics capabilities is preferred.Global business experience is preferred.At Johnson...Full timeLocal areaImmediate start$178k - $307.05k
...our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate... ...representative bodies, as may be required, regulatory approvals and other customary conditions... ....About DePuy SynthesDePuy Synthes is a global leader in Orthopaedics, advancing...Full timeWork at officeLocal areaImmediate start- ...teams to mitigate risks across sites and suppliers. The role offers high visibility to senior leadership and requires strong leadership, regulatory and incident response experience across multi-site operations. Travel limited. #J-18808-Ljbffr Johnson & Johnson MedTech
$122k - $245k
...expertise in Innovative Medicine and MedTech, we are uniquely positioned... ...be considered as a single submission. The Operational Risk Lead... ...risk programs align with regulatory, quality, audit, and Enterprise... ...environment. Strong understanding of global supply chains, supplier risk,...Local areaImmediate start
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