Senior Medical Device Regulatory Lead (U.S./Canada)
V R Della Infotech Inc
V R Della Infotech Inc in California is seeking a Sr. Regulatory Affairs professional to develop regulatory plans and provide guidance to product teams. The role demands a minimum of 8 years of experience in regulatory affairs within the medical device sector, along with a deep understanding of U.S. and Canadian regulations. Candidates should possess strong communication skills and the ability to manage multiple projects effectively. A B.S. in Biomedical Engineering or related field is required, with preference for advanced regulatory qualifications. #J-18808-Ljbffr V R Della Infotech Inc
- BioRobotics is seeking a Senior Regulatory Affairs Specialist at their California headquarters... ...urological surgery innovations. You'll lead cross-functional teams, develop... ...in driving continuous improvement for medical devices. Join us to make a meaningful difference...SeniorRegulatoryMedical device
$148.55k - $174.77k
## Senior Regulatory Affairs SpecialistApplylocations: California... ...science for medical robotics. Your mission... ...modified Class II and III devices and preparing and submitting... ...Involve*** Act as a lead regulatory... ...international standards for U.S. and Rest of World (...SeniorRegulatoryMedical device$148.7k - $297.3k
...the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded... ...processes, quality, attainment, and regulatory compliance.* Develops and... ...Assure line of communication with Senior Leaders on critical delivery issues...SeniorRegulatoryMedical deviceShift work$7.82k - $10.73k
...food, cosmetics, drugs, medical devices, and industrial hemp... ...and reducing risks. The Senior Environmental... ...Enforcement Section (DMDCES) regulatory inspection technical expert... ...incumbent serves in a lead capacity, reviewing... ...Branch (FDB) and the U.S. Food and Drug...SeniorRegulatoryMedical devicePermanent employmentFull timeContract workRemote work$90k - $180k
...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...and peripheral stents. This Senior Regulatory Affairs Specialist position is... ...international markets (e.g., China, Canada, Australia, Brazil)....SeniorRegulatoryMedical deviceWork experience placementWorldwideShift work$105k - $120k
...Diagnostics, creating a world‑leading in vitro diagnostics company... ...future for all. The Role Senior Regulatory Affairs Specialist. This role... ...new in vitro diagnostics and medical devices worldwide. Responsibilities... ...include reviewing and approving U.S. and IVDR regulatory...SeniorRegulatoryMedical deviceWork experience placementWork at officeRemote workWorldwideHome officeNight shift- ...Resources, Inc ( IRI ) Lead Recruiter at... ...sciences, or related medical/scientific field Clinical... ...within a medical device industry Experience... ...(GCP) and/or regulatory compliance guidelines... ...exciting role as a Senior Clinical Research Specialist... ...Remote within the U.S; preferred...SeniorRegulatoryMedical deviceContract workRemote work
$135.1k - $225.1k
...Compliance, this role will lead the North America... ...functionally with commercial, medical/clinical, regulatory, legal, and HR teams... ...‑to‑end execution of U.S. transparency... ...function within the medical device or pharmaceutical... ...AdvaMed Code, MedTech Canada, and OIG/DOJ guidance....SeniorRegulatoryMedical deviceHome officeFlexible hours- ...Position Overview The Senior Medical Affairs Specialist... ...United States, Canada, and other English... ...closely with Regulatory, Marketing, Legal,... .... Stay current on U.S. and Canadian regulatory... .../medical device industry in the U.... ...innovative, industry‑leading organization committed...SeniorRegulatoryMedical deviceWork at officeRemote workHome office
$75.1k
About the Role Senior Product Analyst - 12 Month Defined Term Position... ...thinking. Ensure compliance with U.S. and international regulatory requirements for medical device complaint handling and... ...end‑user customers. Support and lead divisional initiatives and strategic...SeniorRegulatoryMedical deviceWork at officeRelocation package3 days per week$100.32k - $125.4k
Senior Specialist, International Regulatory Affairs Job ID: 164201 Advanced Bionics is seeking a Senior Specialist... ...activities for Class III medical devices. This role is responsible for helping... ...strategy and guidance for outside U.S. and EU markets, including MENA,...SeniorRegulatoryMedical deviceTemporary workWork experience placementWork at officeLocal areaFlexible hours$90k - $180k
Abbott Laboratories in California is seeking a Software Test Engineer to lead verification efforts in a regulated medical device environment. The position includes ensuring product quality, regulatory compliance, and developing robust testing strategies. Required...SeniorRegulatoryMedical device- PROCEPT BioRobotics in California is seeking a Staff Regulatory Affairs Specialist to lead regulatory initiatives for medical robotics, focusing on compliance and innovation... ...in regulatory submissions for medical devices, and strong problem-solving skills. Join us to...RegulatoryMedical device
- Sonova Group is seeking a Senior Specialist in International Regulatory Affairs to support global regulatory activities for Class III medical devices. This role is essential for obtaining and maintaining regulatory approvals across international markets, coordinating with...SeniorRegulatoryMedical deviceLocal area
$7,820 - $10,732 per month
The California Department of Public Health is seeking a Senior Environmental Scientist (Specialist) to lead regulatory inspections for drug and medical devices. This role requires a deep understanding of safety laws and the ability to mentor and train inspectors on regulatory...SeniorRegulatoryMedical device- ...Portfolio. This position is crucial in ensuring patient safety and regulatory compliance while maintaining product quality. Ideal... ...background in product management with a strong understanding of the medical device landscape. The role follows a hybrid work model requiring at...SeniorRegulatoryMedical deviceWork at office
$80 - $100 per hour
...range $80.00/hr - $100.00/hr Quality, Regulatory & R&D Staffing Expert | Contract & Permanent... ...Class III MedTech business to hire a Senior Regulatory Affairs Specialist (... ...Managing a wide variety of RA tasks across Medical Devices Ensuring compliance with Class III device...SeniorRegulatoryMedical deviceHourly payPermanent employmentFull timeContract workFor contractorsRemote work- Intuitive is seeking a CMS Team Manager to lead a unit of DITA Information Architects... ..., you will develop and manage global medical device content while partnering closely with cross... ...high-quality documentation aligns with regulatory requirements while delivering strategic...RegulatoryMedical device
$75.1k - $142.6k
Boston Scientific Gruppe is seeking a Senior Product Analyst for a 12-month defined term position. The role, based hybrid... ...minimum of 3 days a week on site, focuses on ensuring regulatory compliance in medical device complaint handling. Candidates should possess a...SeniorRegulatoryMedical device3 days per week- A leading medical device company is seeking a Senior QA Auditor in California, responsible for planning, executing, and documenting audits, focusing on ISO... ...certification, alongside a history of managing audits with regulatory bodies. #J-18808-Ljbffr Boston Scientific GruppeSeniorRegulatoryMedical device
- Elevait Solutions is seeking a Senior Third-Party Risk Analyst to lead comprehensive risk assessments for vendors, ensuring cybersecurity compliance and regulatory adherence. The ideal candidate will have over 6 years of experience in risk management and be fluent in frameworks...SeniorRegulatory
$157.59k - $203.94k
Scorpion Therapeutics is seeking a Senior Manager, CMC Regulatory Affairs for Biologics based in California... ...candidate will be responsible for leading CMC regulatory efforts, managing regulatory... ...stock incentives, and comprehensive medical benefits. #J-18808-Ljbffr Scorpion...SeniorRegulatory- Eocene Environmental Group, Inc. seeks a Senior Aquatic Resources Specialist to provide a variety of wetland services, including delineations... ...relevant experience, particularly in wetland delineation and regulatory processes. The role requires excellent communication skills and...SeniorRegulatory
- ...Inc. is hiring a Principal GRC Analyst to lead the build-out of compliance and risk... ...environment. The role requires 9+ years of senior experience in GRC and hands-on ISMS experience... ...should have robust knowledge of regulatory frameworks and possess relevant certifications...SeniorRegulatoryRemote job
- ...Function of Position The Sr. Regulatory Affairs primary... ...regulatory strategies for the U.S. and Canadian markets... ...changes. Influence and lead global regulatory... ...pre-submissions, Health Canada submissions with minimal... ...working in a medical device company (can be in combination...RegulatoryMedical device3 days per week
$132k - $172k
Scorpion Therapeutics is seeking a Senior Manager, Medical Writing responsible for authoring and managing regulatory documents. This role requires 7+ years of experience in medical/regulatory writing within the biotech or pharma sectors and strong leadership skills. The...SeniorRegulatory- Fortrea is seeking a Senior CRA II for their FSP team based out of California, focusing on site monitoring and management for clinical... .... The role includes responsibilities such as ensuring regulatory compliance and preparing trip reports, with 60-80% travel requirements...SeniorRegulatory
- Prolacta Bioscience is seeking a Sr. Regulatory Affairs Specialist for their IT Department. This role is vital in supporting regulatory compliance for advertising and promotional materials. You will review and provide input on claims and labeling, ensuring alignment with...SeniorRegulatoryFixed term contract
- A leading clinical research organization is seeking a Senior Clinical Trial Manager to oversee the end-to-end execution of clinical trials, specifically in oncology... .... The ideal candidate will ensure compliance with regulatory requirements and collaborate across functions to...SeniorRegulatory
$115k - $125k
Capio Group is seeking a Business Analyst Lead to implement a cloud-based SaaS licensing platform. The role involves project planning... ...have significant experience in the IT field, especially with regulatory systems. This full-time remote position offers a salary between...SeniorRegulatoryRemote jobFull time
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