Global Regulatory Operations Lead - Medical Devices
Siemens Healthineers
Varian Medical Systems, a Siemens Healthineers company, is seeking a Regulatory Operations Manager in Palo Alto, CA. You will lead a small global team, govern market clearance, and drive digitalization of regulatory processes to ensure FDA, EU MDR, Health Canada compliance and timely product availability. Collaborate with Quality, Legal, Engineering, and Marketing, influence cross-functional programs, and mentor staff to achieve regulatory excellence across the portfolio. #J-18808-Ljbffr Siemens Healthineers
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Global Regulatory Operations Lead - Medical Devices in Palo Alto, CA vacancy
- Varian Medical Systems, a Siemens Healthineers company, is seeking a Regulatory Operations Manager to lead global regulatory operations in support of market access and regulatory requirements for its medical device portfolio. The role oversees regulatory systems, data,...RegulatoryMedical device
- Pulmonx Corporation, a medical device company leading in COPD therapies, seeks a Senior Marketing Operations Specialist to manage global marketing collateral, ensure brand consistency, and support regulatory compliance. You will coordinate material reviews, expense tracking...RegulatoryMedical device
- ...Group is seeking an experienced Vice President of Regulatory Affairs & Quality to lead regulatory strategies for medical devices. This role requires a minimum of 15 years of... ..., and representing the company before global agencies. #J-18808-Ljbffr Russell Solutions GroupRegulatoryMedical device
- ...do at Intuitive. As a global leader in robotic-... ...Function of Position CDE Operations (CDE Ops) Lead position reports to... ...and all applicable regulatory and institutional lab... ...B.S. in technical or medical fields with project management... ...level: AssociateIndustry: Medical DeviceRegulatoryMedical deviceLocal areaWorldwideFlexible hours
- A leading health technology firm is seeking a Regulatory Affairs Specialist to manage regulatory submissions and compliance activities for innovative medical devices. The ideal candidate will have a Bachelor’s degree and significant experience in the medical device industry...RegulatoryMedical device
- Intuitive in Sunnyvale, CA seeks an experienced Regulatory Affairs professional to provide expert leadership in global submissions and compliance strategy. The role focuses on cross-functional coordination, technical documentation, and agency interactions to support product...RegulatoryMedical deviceWorldwide
$101k - $187.6k
...Project Management Chapter, the Global Project Manager (GPM) plays a... ...), etc., as applicable & may lead improvement initiatives. You... ...in the diagnostic, medical device, pharmaceutical or biotech industry... ...and clinical validations and regulatory submissions or instrument development...RegulatoryMedical deviceFull timeLocal areaRelocation package$162.5k - $286.8k
...at Intuitive . As a global leader in robotic-... ...Support teams. This role leads a team of business... ...governance to drive operational excellence, customer... ...initiatives across a global medical device organization. This... ...with applicable regulatory requirements, including...RegulatoryMedical deviceFull timeContract workLocal areaWorldwideFlexible hoursShift work- Google seeks a senior Regulatory Affairs lawyer to lead a new Standards, Operations, and Scaled Resolution team. You will guide regulatory strategy, advise on AI-enabled matter management, and scale compliant workflows across the organization. The role sits at the nexus...Regulatory
- Nclusion, based in Palo Alto, is seeking a Product Ops Lead - Payments to own the rollout and operation of remittance corridors across markets. You will... ...with Country GMs on expansion sequencing, ensuring regulatory clearance and partner readiness for scalable, compliant...Regulatory
$162.5k - $286.8k
...at Intuitive . As a global leader in robotic-assisted... ...productivity, operational efficiency, and business... ...The Senior Manager will lead a team focused on AI... ...Partner with Quality, Regulatory, Legal, Privacy, and Cybersecurity... ...~ Experience in the medical device, healthcare, life...RegulatoryMedical deviceFull timeLocal areaWorldwideFlexible hoursShift work$114k - $228k
...AmericaTime Type: Full timeAbbott is a global healthcare leader that helps... ...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded... ...Product Development, Quality, Ops, Regulatory organizations to support...RegulatoryMedical deviceShift work$114k - $228k
...Date: 2026-08-03Abbott is a global healthcare leader that... ...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...Clinical, Medical Affairs, Regulatory, Quality, Operations, Supply Chain,...RegulatoryMedical deviceLocal areaWorldwide$143.3k - $236.5k
Sr Product Manager - Global Service Portfolio Role... ...service offering lifecycle. Operating with significant... ...Digital/IT, Quality, and Regulatory. Partners with... ...upsell, and adoption. Lead end‑to‑end lifecycle governance... ...environments (e.g., medical devices, diagnostics, life...RegulatoryMedical deviceContract workLocal area- Abbott is hiring a Regulatory Affairs Specialist for their Vascular Division in Santa Clara, CA. This role focuses on supporting EU and US regulatory activities for endovascular medical devices used in treating peripheral artery disease. Ideal candidates should possess...RegulatoryMedical device
- System One is seeking a Sr. Regulatory Affairs Specialist in Sunnyvale, CA. The role... ...of Regulatory Affairs experience in medical devices. You will lead regulatory plans, prepare FDA 510(k)... ...with international teams to support global submissions and drive cross-...RegulatoryMedical device
- System One is seeking a Regulatory Affairs Specialist IV in Sunnyvale, CA, to lead regulatory strategy and submissions for medical devices across the U.S., Canada, and global markets. This 6‑month contract role requires deep regulatory expertise and strong cross‑functional...RegulatoryMedical deviceContract work
$144k - $209k
...efficient way to use QMS to meet regulatory expectations.Create a system... ..., Computer Science, Operations, a related technical field,... ...architecture for software as a medical device or digital health products.Experience... ....Experience engaging with global health authorities or...RegulatoryMedical deviceShift work- Google is seeking a Regulatory Affairs senior leader to guide strategy and operations for global regulatory initiatives in the US. You will partner with Public Policy, Legal... ...regions. In this role, you will drive OKRs, lead strategic planning, and coordinate complex regulatory...Regulatory
$219k - $305k
...experience in management consulting, operations, business strategy, regulatory, legal or corporate advisory, or 8... ...restructuring. Experience in leading teams and managing people in a matrix... ...world. We partner with teams across global affairs, product areas, and the rest...RegulatoryTemporary work$112k - $168k
...process control, combining global scale with an expanded portfolio of leading-edge technologies that... ...most difficult yield, device performance, quality,... ...lead the end-to-end trade operations strategy & execution... ...fiscal efficiency and regulatory adherence. Key Responsibilities...RegulatoryPermanent employment$120.04k - $153.49k
SupportFinity™ is seeking an Associate Director, Global Operations to lead and improve global hiring, training, and HR processes. This role manages annual project planning for the Transformation Program recruitment and serves as the risk management lead. The ideal candidate...$194k - $223k
...revolutionize patient care globally through transformational, accessible... ...for you. Responsibilities:Lead the technical launch of... ...objectives, clinical needs, and regulatory requirements. Prioritize... ...unlocked new use cases for medical devices. Physical Demands:This is a...RegulatoryMedical deviceWork visaNight shiftWeekend work3 days per week$145k - $167k
...revolutionize patient care globally through... ...RoleJob Title: Senior Regulatory Affairs SpecialistLocation... ...strategy for the company’s devices and ensures compliance... ...teams and leadership.Lead the preparation of all... ...approaches.Strong knowledge of medical device labeling...RegulatoryMedical deviceWork experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week$110k - $130k
...exploration and life-saving medical devices to building... ...America, we partner with leading companies in... ...more. As part of the global ALTEN Group—57,000+ engineers... ...ensure products meet regulatory, safety, and... ...precision. The team operates an onsite test laboratory...RegulatoryMedical deviceFor contractorsImmediate startALTEN Technology USA
Mountain View, CA16 days ago$291.72k - $343.2k
...OF JOB As Vice President of Regulatory Affairs, you will oversee... ...know regulatory road maps for medical devices and preferably combination drug... ...the regulatory strategy globally and be the key point person... ...Develop and implement the annual operating and capital budgets to meet...RegulatoryMedical deviceTemporary workSight Sciences Inc
Menlo Park, CAmore than 2 months ago- ...on-demand delivery and is looking for a Senior Director of Global Operations to lead and scale its drone delivery service from Palo Alto or... ...contractors, and drive AI-enabled scheduling, ensuring safety and regulatory compliance while expanding to new markets. #J-18808-...RegulatoryFor contractorsRemote work
$155k - $175k
...and resolving serious unmet medical needs. At Summit, we believe... ...Oncology. Summit Has Multiple Global Phase 3 Clinical Studies, Including... ...presently approved by any regulatory authority other than China’s... ...Collaborations Business Operations, is an action-role delivering...RegulatoryFull timeSummit Therapeutics, Inc.
Palo Alto, CA18 days ago- The Vice President Regulatory Affairs & Quality will be an experienced professional... ...a track record of success in the medical device industry. The responsibilities of... .... This person will drive the global regulatory affairs strategy, leading the execution of regulatory...RegulatoryMedical device
$210k - $245k
...resolving serious unmet medical needs. At Summit, we... .... Summit Has Multiple Global Phase 3 Clinical Studies... ...approved by any regulatory authority other than China... ...Collaborations Business Operations & Strategy, is a... ...the primary operational lead for partner-sponsored...RegulatoryFull timeContract workSummit Therapeutics, Inc.
Palo Alto, CA18 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Global Regulatory Operations Lead - Medical Devices. Be the first to apply!
Related searches
- operations leader Palo Alto, CA
- operations lead Palo Alto, CA
- clinical research regulatory Palo Alto, CA
- regulatory law Palo Alto, CA
- regulatory scientist Palo Alto, CA
- regulatory technician Palo Alto, CA
- regulatory Palo Alto, CA
- regulatory cmc Palo Alto, CA
- regulatory engineer Palo Alto, CA
- regulatory accountant Palo Alto, CA