Senior Global Regulatory Strategist - Medical Devices
Getinge
Getinge is seeking a Regulatory Affairs professional in Wayne, New Jersey, to handle compliance activities. The role involves preparing regulatory strategies for new devices and managing submissions, including 510(k) and PMA approvals. Candidates must have a Bachelor’s Degree and significant experience in medical devices, alongside strong analytical and negotiation skills. The position offers the opportunity to work cross-functionally and contribute to compliance documentation. #J-18808-Ljbffr Getinge
$172k - $275.2k
Regulatory Affairs Strategist, Globalization Job Description The Regulatory Affairs Strategist, Globalization,... ...Minimum 8 years of experience in the medical device industry, with at least 5 years... ...problems and recommendations to senior management effectively and...SeniorRegulatoryMedical deviceDaily paidTemporary workWork at officeLocal areaWorldwideFlexible hours- BD is seeking a Regulatory Affairs Strategist, Globalization, to guide worldwide regulatory affairs strategies in Franklin Lakes, New Jersey. This role... ...s degree with at least 8 years of experience in the medical device industry, including 5 years in Regulatory Affairs....SeniorRegulatoryMedical deviceWorldwide
- ...Getinge in Wayne, New Jersey is seeking a Senior Compliance Engineer. This role involves ensuring that electromechanical medical devices comply with global regulatory, quality, and safety standards throughout their lifecycle. Key responsibilities include leading compliance...SeniorRegulatoryMedical device
- ...Getinge is seeking a Senior Compliance Engineer in Wayne, NJ to ensure that Cardiac Assist medical devices meet global regulatory and safety standards. Responsibilities include leading compliance evaluations, supporting product designs, and collaborating with multiple...SeniorRegulatoryMedical device
$121k - $181k
...Role As an R&D Category Senior Associate, you will... ...innovation across Reckitt’s Global VMS (Vitamins, Minerals... ..., Clinical, and Regulatory teams. Responsibilities... ...development and execution of medical and evidence strategies... ..., medical device, or similar industries...SeniorRegulatoryMedical deviceTemporary workInternship$137.1k - $181.65k
Join to apply for the Senior Manager, Global Design Assurance role at embecta 1 week ago Be among... ..., will lead and build a dynamic medical device design assurance team focused on standardizing... ...specifically R&D, Quality Systems, Regulatory Affairs, Operations Quality, and...SeniorRegulatoryMedical deviceFull timeWorldwide- ...A leading medical technology company is seeking a Sr. Quality Engineer in Wayne, NJ. This... ...processes, maintaining compliance with regulatory standards, and leading continuous improvement... ...Engineering, especially in the medical device sector. Key qualifications include a...SeniorRegulatoryMedical deviceWork from home
- ...components for submission to regulatory agencies, participation... ..., private labels, device/combination products... ...labeling strategy proposal (Global Regulatory Affairs,... ...Pharmacovigilance, Global Medical Affairs, Legal,... ...Proficient in presenting to senior management when required...SeniorRegulatoryLocal area
- ...BD is one of the largest global medical technology companies in the... ...Job Description The Regulatory Affairs Strategist, Project Management, is responsible... ...within a medical device industry or similar regulated... ...problems and recommendations to senior management effectively......RegulatoryMedical deviceDaily paidTemporary workWork at officeRemote workFlexible hours
$137.5k - $220.1k
...BD is one of the largest global medical technology companies in the... ...Job Description The Regulatory Affairs Strategist, Project Management, is responsible... ...within a medical device industry or similar regulated... ...and recommendations to senior management effectively......RegulatoryMedical deviceHourly payDaily paidTemporary workWork at officeRemote workFlexible hoursShift work- ...Position : Senior Manager, EU MDR/IVDR Location :... ...Manager, EU MDR/IVDR, Medical Governance and Analytics... ...collaborate with parts of the Global Medical Safety organization as well as Regulatory and Quality to ensure... ...for medical devices and IVDs. Demonstrated...SeniorRegulatoryMedical deviceContract workWork experience placement
$120k - $135k
...home (site based) Salary Range: $120k – 135k Job Overview The Senior Compliance Engineer is responsible for ensuring that Cardiac Assist electromechanical medical devices meet all applicable global regulatory, quality, and safety requirements throughout their lifecycle....SeniorRegulatoryMedical deviceTemporary workRemote workWork from homeFlexible hours$132k - $221k
...days) to receive an alert: Create Alert Senior Product Manager, Global Marketing – CNS Cancers Chesterbrook, PA... ...and collaborate with Regional Marketing, Medical Affairs, Patient Experience, Clinical Development, and Regulatory teams Track competitive intelligence and...SeniorRegulatoryPermanent employmentFull timeWork at officeLocal areaFlexible hours3 days per week- A medical device organization is seeking a Senior Quality Control Engineer to ensure compliance with quality, safety, and regulatory requirements for orthopedic implants. The role involves leading inspection processes, driving continuous improvement initiatives, and mentoring...SeniorRegulatoryMedical device
- ...Belgium in Parsippany-Troy Hills seeks a professional for device lifecycle management of medical devices. You will develop risk management plans and... ...design changes, collaborating with both engineering and regulatory teams. The ideal candidate is well-versed in Device Design...SeniorRegulatoryMedical device
- JPMorganChase is looking for a Senior Home Lending Advisor to serve as the primary contact for customers throughout the loan process.... ...collaboratively promote mortgage products while maintaining compliance with regulatory standards. This role requires a bachelor's degree, 3+ years of...SeniorRegulatory
- ...Contract position for a Senior Mechanical Engineer / Principal Engineer for design and development of electromechanical medical devices. Review and helps to develop product specifications... ...requirements such as environmental, regulatory and safety requirements. Generate...SeniorRegulatoryMedical deviceContract work
$120k - $170k
...currently offer over 600 clinically relevant medical devices to healthcare providers, including... .... Learn more at Scope The Manager, Global CAPA System is responsible for the governance... ...fully compliant with applicable global regulatory requirements, including but not limited...RegulatoryMedical deviceWork at office- Becton Dickinson is seeking a Regulatory Affairs Specialist, Digitalization to manage regulatory documentation and improve digital platforms... ...relevant field and has at least 3 years of experience in the Medical Device industry. This role involves collaborating across teams to...RegulatoryMedical device
- ...A global medical technology company located in Wayne, NJ is looking for a Principal Product Manager & Team Lead. This senior role involves overseeing a complex cardiovascular surgery product portfolio... ...have over 10 years in medical device management and demonstrated...SeniorMedical deviceRemote work2 days per week1 day per week
- ...in close alignment with the global tax strategy. Identify, evaluate... ..., and the changing regulatory landscape. Ensure all tax aspects... ...effectively relate tax issues to senior leadership; demonstrated understanding... ...found at the intersection of medical science and digital...SeniorRegulatoryFull timeLocal areaShift work
- BD is seeking a Regulatory Affairs Strategist in Franklin Lakes, NJ. This role involves project management and optimizing processes within Regulatory... ...of experience in Regulatory and Quality, focusing on medical devices. Benefits include competitive salary, bonuses, and...RegulatoryMedical device
- ...Senior Technical Associate, Quality Assurance As a privately-owned, biopharmaceutical... ..., and helps develop SOPs aligned with regulatory expectations. The position also... ...and gene therapy, such as GMP, ISO, or medical device development. Knowledge of standard industry...SeniorRegulatoryMedical deviceWork at office
- ...international compliance activities. Prepare comprehensive regulatory strategies for new devices and post market changes. Clearly communicates strategies... ...directly related experience in Regulatory Affairs in a medical device environment, or a minimum ten years of directly...SeniorRegulatoryMedical deviceWorldwide
- ...Job Title – Senior Clinical Data Manager Location - Franklin Lakes, NJ Duration... ...: 8am-5pm, 40 hours/week Client: Medical Device Company Employment Type: Contract on... ...Understands clinical research process and regulatory requirements. Able to acquire and...SeniorRegulatoryMedical deviceContract workLocal areaRemote work
$170k - $185k
...embecta is a global diabetes care company that is leveraging its... ...operational excellence, regulatory compliance, and long-term business... ...Must have experience out of medical device/pharmaceutical manufacturing... ...manner to embecta senior management Strong knowledge...SeniorRegulatoryMedical deviceWork at officeLocal areaRemote work- Senior Manager, PAQ Virology Strategy (US Medical Affairs) — Patient Access and Quality of Care (PAQ) Responsibilities... ...1+ year Medical Affairs (pharma/device), managed care, or HEOR... ...urgent, fast‑paced environment Solid regulatory/compliance knowledge Strong organizational...SeniorRegulatoryMedical device
- ...Senior Associate, Data Scientist Join our Global Real Estate (GRE) Design & Construction (D&C) team and help shape the future of workplace insights at... ...integrity, with demonstrated commitment to compliance with regulatory obligations Preferred qualifications,...SeniorRegulatory
$100k - $125k
...Job Description Senior Technical Associate, Quality Assurance ensures compliance with... ...audits, and helps develop SOPs aligned with regulatory expectations. The position also... ...and gene therapy, such as GMP, ISO, or medical device development. Knowledge of standard industry...SeniorRegulatoryMedical deviceFull timeTemporary workWork at officeLocal area$120k - $135k
...technical leadership in the development, optimization and sustaining of manufacturing processes for medical devices in accordance with Getinge’s Quality system and regulatory requirements (ISO 13485 and FDA 21 CRF Part 820). This individual is a key resource during...SeniorRegulatoryMedical deviceTemporary workWorldwideFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Global Regulatory Strategist - Medical Devices. Be the first to apply!
- senior manager quality engineering Wayne, NJ
- senior performance engineer Wayne, NJ
- senior manager diversity & inclusion Wayne, NJ
- senior cybersecurity engineer Wayne, NJ
- senior manager m&a tax Wayne, NJ
- senior accountant remote Wayne, NJ
- senior level Wayne, NJ
- senior software engineer remote Wayne, NJ
- senior ux designer remote Wayne, NJ
- senior international tax analyst Wayne, NJ

