Regulatory Specialist Sr
Abbott Laboratories
Title : Regulatory Specialist Sr Location : Santa Clara, California, 100% Onsite Duration : 12 months Summary The ideal candidate operates with a high degree of independence, demonstrates strong cross-functional leadership, and can manage complex, multi-stakeholder deliverables with minimal oversight. Key Responsibilities Tender Coordination & Execution Lead and own end-to-end global tender regulatory deliverables, including regulatory documentation, certifications, and product compliance data Serve as the central point of accountability for tender-related regulatory activities across franchises Drive alignment and coordinate inputs across SMEs, including international affiliates, manufacturing, quality, packaging, R&D, and labeling teams Develop and manage tender trackers, timelines, and governance structures to ensure visibility and on-time execution Identify risks, proactively elevate issues, and implement mitigation strategies to ensure tender success and timeliness Ensure compliance with regional and country-specific regulatory requirements. Develop and monitor KPIs and dashboards to track performance and drive continuous improvement Regulatory Operations & Documentation Lead the review, coordination, and tracking of regulatory letters (LoA, PoA, controlled substance letters, evidence of conformance, etc) Executes preparation and submission of Certificates to Foreign Governments (CFGs), CFG-NE, COEs in the FDA database Provide oversight and quality review of Declarations of Conformity (DoC), DoC templates, and translations, ensuring compliance with MDR and global standards and regulations. Support translation requests through the translations portal. Review EU MDR DoC translations for accuracy and consistency Ensure adherence to Good Documentation Practices (GDP) across all deliverables Executes and tracks addendum labeling requests Cross-Functional Leadership Act as a key liaison between Regulatory Affairs, Quality, Supply Chain, Legal, and international affiliates to resolve complex regulatory challenges Facilitate cross-functional governance meetings and drive decision-making and accountability Influence stakeholders and align priorities across multiple functions and geographies Process Improvement & Governance Identify and implement process improvements and automation opportunities within regulatory operations and tender workflows Lead and support change management activities, including updates to procedures, templates, and systems Maintain and enhance trackers, SharePoint repositories, and documentation systems to improve efficiency Compliance & Issue Management Identify and address compliance risks and quality system gaps Support CAPA investigations and remediation activities Troubleshoot and resolve regulatory operational challenges impacting deliverables Qualifications Proven experience in Regulatory Affairs, Regulatory Operations, or international submissions Strong experience managing complex, cross-functional initiatives independently Demonstrated expertise in global regulatory requirements (e.g., EU MDR, international markets) Advanced project management, prioritization, and organizational skills Excellent stakeholder management and influencing skills, including the ability to drive alignment without direct authority Strong critical thinking and problem-solving capabilities Ability to operate with minimal oversight and high accountability for outcomes. Consultants Eligible Benefits Upon Waiting Period Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account (for High-Deductible Health Plans) Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit) Supplemental Life Insurance Short Term Disability (coverage varies by state) Long Term Disability Critical Illness, Hospital coverage, Accident Insurance MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs. #J-18808-Ljbffr Abbott
$171k - $231.4k
...Fire tablets, Fire TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in class products.The ideal candidate will have experience building a regulatory...SeniorFor contractorsLocal areaFlexible hours$47 - $51 per hour
...Job Description Job Description Sr Regulatory Affairs Specialist, Global Market Protection Location : Remote Shift : M-F, standard working hours Pay : $47/hr-$51/hr 1 year contract role Overview: The Regulatory Affairs Senior Specialist is responsible...SeniorContract workTemporary workWork experience placementLocal areaRemote workShift work- ...to embark on an exciting journey that will revolutionize the way men suffering from BPH are treated? Join us as a Senior Regulatory Affairs Specialist and be at the forefront of regulatory science for medical robotics. Your mission? To support a deep culture of...SeniorFull time
- ...DescriptionPrimary Function of Position This role provides expert support for regulatory project management, strategic submissions, and cross-... ...and documentation. • Mentor and coach regulatory affairs specialists. • Track and report metrics on regulatory timelines and...SeniorLocal areaWorldwideFlexible hours
$117k - $144k
...storage, and data center manufacturing and distribution activities. This role is responsible for coordinating FTZ customs processes, regulatory compliance activities, and operational execution associated with high-volume import/export activity across multiple FTZ locations...SeniorWorldwide$90k - $180k
...States > Santa Clara : Building A - SCJob Type: Full timeCategory: Regulatory AffairsIndustry: HealthcarePosted Date: 2026-07-17Abbott is a... ...contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure...SeniorWork experience placementWorldwide$90k - $180k
...balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, or Temecula, CA locations in the Abbott Vascular Division...SeniorWorldwideShift work$55 - $60 per hour
...Job Title: Sr. Regulatory Affairs Specialist Location: Sunnyvale, CA, United States Type: Contract Compensation: $55.00 - $60.00 Work Model: Hybrid Overview Established Medical Device company is looking to hire a Sr. Regulatory Affairs...SeniorContract workLocal area- ...Senior Regulatory Affairs Specialist It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30... ..., you'll find your purpose here. Job Description The Sr. Regulatory Affairs Specialist's primary responsibilities include...SeniorLocal areaWorldwideFlexible hours
- ...Function of Position: This role provides expert support for regulatory project management, strategic submissions, and cross-functional... ...and documentation. Mentor and coach regulatory affairs specialists. Track and report metrics on regulatory timelines and success...SeniorLocal areaWorldwideFlexible hours
$92.7k - $152.9k
Job Description Summary Sr. International Regulatory Affairs Specialist to join our Regulatory Affairs team. Responsible for preparing and managing regulatory submissions to support global commercialization of new or modified IVD devices and RUO products. Key Job Responsibilities...SeniorWork experience placementLocal area- ...transformative opportunities that provide continuous career growth opportunities.The Opportunity That Awaits You: The Principal Regulatory Affairs Specialist provides regulatory leadership for product manufactured by PROCEPT BioRobotics (“company”) from development through...Full timeWork at office
$100k - $200k
...vessel closure devices and peripheral stents.The Opportunity Abbott is seeking a highly motivated and experienced Principal Regulatory Affairs Specialist to join our Vascular Division team on-site in Santa Clara, CA or Temecula, CA. In this role, you will provide regulatory...For contractorsShift work$150k - $250k
DescriptionOverview :Responsible for design, development, and refinement of Multi-Gbps PAM4 SerDes IP. Design and debug experience on RTL level signal synchronization, clock tree and cross domain clock designs is a significant plus.Need to work closely with system and test...Senior$97.6k - $137.25k
Worker Sub-Type:RegularJob Description: This role will report into the Director of Internal Audit and SOX Compliance within the Finance organization and is integral to the company’s financial reporting integrity, risk management strategy, and operational resilience. This...SeniorFull timeWork at officeRemote work- Category (For Job Seekers)Information TechnologyLocation11201 - PCB San Jose CA USA - San Jose, CA 95131 US13147 - EMS Colorado Springs CO USA - Colorado Springs, CO 80918 US13631 - ISS Austin Texas US - Austin, TX 78754 US15551 - EMS Carrollton TX US - Carrollton, 7500...SeniorWork at office
$145k - $167k
...relevant diagnostic imaging. Learn MoreAbout The RoleJob Title: Senior Regulatory Affairs SpecialistLocation:Palo Alto, CA or Guilford, CT (Hybrid, 3 days/week)The Senior Regulatory Affairs Specialist advises regulatory strategy for the company’s devices and ensures...SeniorWork experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week- ...Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. The client seeks a Principal Regulatory Affairs Specialist to lead complex regulatory strategies and submissions for Class III implantable devices and software-driven technologies...
$81.5k - $141.3k
...and software, vessel closure devices and peripheral stents.The Opportunity Abbott is seeking a passionate, experienced Regulatory Affairs Specialist to join our Vascular Division team on-site in Santa Clara, CA or Temecula, CA. In this role, you will support EU and US...For contractorsShift work$154k - $286k
At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology.Work with the Cadence global silicon solutions teams who are designing semiconductor IP for the top electronic product companies in the world, in leading edge semiconductor...SeniorFull time$188k - $325k
About GlobalFoundries:GlobalFoundries is a leading full-service semiconductor foundry providing a unique combination of design, development, and fabrication services to some of the world’s most inspired technology companies. With a global manufacturing footprint spanning...SeniorFull timeLocal area- ...can create a brighter, more sustainable future while tackling the most pressing challenges of the 21st century.We are looking for a Sr. Principal Electrical Engineer, Microgrid Modeling to join our team in one of today’s most exciting technologies. This role will report...SeniorFull timeWork at officeWorldwide
$103.6k - $155.4k
...impossible. Our employees are not only part of history, they're making history.Northrop Grumman Mission Systems is looking for a Principal /Sr.Principal Metrology Engineer CMM located in Sunnyvale, CA.What you'll get to do:Properly evaluate and interpret engineering models,...SeniorFull timeRelocation packageShift work$223.66k - $313.06k
...About the Opportunity The Sr Data Scientist, Risk will offer a strategic perspective, deep analytical and modeling capabilities, and a collaborative working style. The right candidate will have strong intellectual curiosity and passion for achieving business results...Senior- ...most pressing challenges of the 21st century.We are looking for a Sr Principal Engineer, Enclosures Design, to join our team in one... ...current and future productsLead and manage the performance and regulatory testingInterpret/develop Tolerance Analysis, CAE, DFM, DFMEA, PFMEA...SeniorFull timeWork at officeWorldwide
$129.3k - $193.9k
...are not only part of history, they're making history.Northrop Grumman Mission Systems (NGMS) is looking for you to join our team as a Sr. Principal Manufacturing Engineer based out of Sunnyvale, CA. You will support the manufacturing and testing of marine launcher...SeniorFull timeWork experience placementRelocation packageShift workWeekend work- ...Our client, a leading organization in the medical device industry, is seeking a Regulatory Specialist to join their team. As a Regulatory Specialist, you will be part of the Regulatory Affairs Operations team supporting international labeling and compliance initiatives...Weekly payTemporary workFlexible hours
$164k - $264.5k
...Status (CRS), Function Level Reset (FLR), and reset separation. Experience with I/O virtualization and isolation technologies such as SR-IOV, SIOV, PF/VF isolation, and related software-visible requirements. Strong understanding of RAS, telemetry, reliability, and...SeniorWork experience placementWork from home- Join Nokia's advanced photonics and semiconductor design team, developing next-generation analog ICs for high-speed optical communication systems. In this role, you will lead the design of multi-tens of GHz Transimpedance Amplifiers (TIAs) for coherent long-haul, metro,...Senior
- ...model supports real-time problem-solving, stronger relationships, and the kind of precision that drives great outcomes.Job SummaryAs a Sr Principal Product Manager for Strata Cloud Manager Platform, you will be responsible for the foundational aspects of our platform,...SeniorFull timeWork at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Specialist Sr. Be the first to apply!
- research compliance officer Santa Clara, CA
- regulatory compliance associate Santa Clara, CA
- regulatory officer Santa Clara, CA
- healthcare compliance officer Santa Clara, CA
- medicare compliance specialist Santa Clara, CA
- regulatory affairs specialist Santa Clara, CA
- compliance specialist Santa Clara, CA
- compliance consultant Santa Clara, CA
- coding compliance specialist Santa Clara, CA
- aml compliance analyst Santa Clara, CA



