Global Regulatory Affairs Specialist - Medical Devices
Abbott Laboratories
Abbott Laboratories in Pleasanton, CA is seeking a Regulatory Affairs Specialist to support regulatory activities and product registrations across the Heart Failure division. This role partners with cross-functional teams and works with limited supervision to ensure timely regulatory submissions. You will review engineering changes, maintain compliance with FDA and international regulations, and help drive lifecycle management while delivering accurate documentation and clear communications. #J-18808-Ljbffr Abbott Laboratories
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Global Regulatory Affairs Specialist - Medical Devices in Pleasanton, CA vacancy
$90k - $180k
...PleasantonJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...: 2026-08-19Abbott is a global healthcare leader that helps... ...and products in diagnostics, medical devices, nutritionals and branded... ...recruiting for a Senior Regulatory Affairs Specialist to join our team on-site in...Medical deviceFor contractorsWorldwide- Abbott is seeking a Regulatory Affairs Specialist for the Pleasanton, CA area to support the Heart Failure... ...approvals and licensing for medical devices. You will interact with regulatory agencies... ..., ensure compliance with FDA and global requirements, and contribute to timely...Medical device
$73.9k - $116k
...Abbott is a global healthcare leader that helps people live more fully at all... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...tomonitoringand treatment. The Opportunity This Regulatory Affairs Specialist will work out of our Pleasanton, CA...Medical deviceWork experience placementShift workAbbott
Pleasanton, CA1 day ago- Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA.... ...We are seeking an experienced Senior Regulatory Affairs Specialist to support our growing Regulatory Affairs... ...experience, working knowledge of global regulatory landscapes, and a...Medical deviceWork at officeWorldwideShift work
$90k - $180k
...PleasantonJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...: 2026-07-10Abbott is a global healthcare leader that helps... ...and products in diagnostics, medical devices, nutritionals and branded... ...Opportunity This Senior Regulatory Affairs Specialist will work out of our...Medical deviceFor contractorsWork experience placementWork at office- ...Overview We are partnering with a growing, innovative medical device organization seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy, submissions, and product lifecycle activities. This is a high-impact opportunity to work cross-functionally...Medical deviceLocal area
LHH
Dublin, CA5 days ago $90k - $180k
...HealthcarePosted Date: 2026-07-22Abbott is a global healthcare leader that helps people... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...teams for concept feasibility and formal regulatory submission Contribute to the continuous...Medical deviceFor contractorsRemote workWorldwide- Stryker, a leading medical device company, is seeking a Global Portfolio Manager to drive strategy for neurovascular devices including thrombectomy... ...will collaborate with R&D, marketing, sales, and regulatory affairs to guide from concept to commercialization and maximize...Medical deviceWork at office3 days per week
- ...possible in cell analysis. As the company continues to scale its global commercial organization and expand the reach of its Solutions... ...experience within life science tools, clinical diagnostics, medical devices, capital equipment, or a related industry. 8+ years of...Medical deviceContract workWork at officeWorldwide
- Abbott in Pleasanton, CA is seeking a Senior Regulatory Affairs Specialist to support worldwide regulatory submissions and compliance. You will partner with cross-functional teams to prepare documentation needed for registrations and ensure ongoing licensing. The role requires...Worldwide
- A medical device company is seeking a Vice President of Operations and Quality Assurance in Pleasanton, CA. This role requires 10+ years... ...quality and operations. The VP will oversee strategic planning, regulatory compliance, and operational excellence initiatives to enhance...Medical device
- ...Pleasanton, CA. You will lead system integration for complex medical devices, focusing on the integration of hardware and software. The ideal... ...environments. This role requires collaboration across global teams to achieve project objectives. Qualifications include a...Medical device
- ...Medical Device AssemblerThe medical device assembler is responsible for producing high-quality medical devices within a manufacturing cell under close supervision. This role may include assembly, repair, and testing of pacemakers, implantable cardioverter defibrillators...Medical device
Equiliem
Pleasanton, CA2 days ago - ...issues today and address the medical challenges of tomorrow. We strive... ...Quality Engineer, Medical Device External Quality is part of... ...with defined specifications and regulatory requirements.... ...Participates in the development of global Product Quality Assurance strategy...Medical deviceFull timeContract workTemporary workLocal area
AbbVie Inc.
Pleasanton, CAmore than 2 months ago - .... Join our team. #CloroxIsThePlaceYour role at Clorox:The Regulatory Affairs Specialist II provides regulatory leadership to support the compliance... ....Monitor regulatory changes (e.g., federal, state, global trends) and translate impacts into actionable changes.Work...Full timeSummer workWork at officeRemote workFlexible hours3 days per week
$172k - $344k
...Pleasanton, United States of AmericaTime Type: Full timeAbbott is a global healthcare leader that helps people live more fully at all... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues...Medical deviceShift work$95.5k - $190.9k
A global healthcare leader is seeking a Scientific Communications Manager in Pleasanton, CA. This role involves leading evidence generation... ...should have a Master's degree and extensive experience in the medical device industry. The position offers a competitive salary range from...Medical device- Abbott is a global healthcare leader focused on improving life through innovative medical devices and therapies. The Clinical Specialist role involves clinical education, procedural support, and collaboration with cardiology teams across a defined region. Travel may exceed...Medical device
$170k - $225k
...precision manufacturing company serving the aerospace, defense, medical device, and space industries is seeking an experienced General... ...leadership benchMaintain compliance with AS9100, ISO 9001, and other regulatory requirementsSupport customer relationships, audits, new...Medical device- ...Summary:Manufacturing Engineer with 3-4 years of experience in the medical device manufacturing industry, specializing in supporting regulated... ...and MES systems while ensuring compliance with quality and regulatory standards.Strong background in cross-functional collaboration...Medical device
- ...Co-op/Intern will support sustaining and new product activities on-site, with a minimum of 20 hours per week for the duration of the program. This role offers exposure to medical device engineering in a collaborative environment. #J-18808-Ljbffr AtriCure Co-op/InternMedical deviceInternship
- Stryker, a global medical technology leader, seeks Mechanical Engineering interns to contribute to meaningful R&D projects across New Product Development, Product Engineering, and Test Lab initiatives. You will apply classroom knowledge in a fast-paced setting and collaborate...Medical deviceInternship
- ...partner with the broader PM team to evolve core capabilities for Medical Device and Diagnostic customers. You will translate complex MedTech... ...AI teams to drive a scalable roadmap and successful customer adoption across global markets. #J-18808-Ljbffr Veeva Systems, Inc.Medical device
- ...investigators and engineers responsible for post-market surveillance and root-cause analysis of complaints. You will partner across Medical Affairs, Regulatory, Operations, R&D and Customer Service to ensure timely, compliant investigations, maintain documentation per FDA/ISO...Medical device
- ...analyzing physiological data, and supporting verification and validation of wearable medical devices. You will collaborate with Clinical Research, Engineering, Quality, Regulatory Affairs, and Product teams, reporting to the Chief Scientific Officer, contributing to next...Medical device
- ...in Pleasanton, CA, is seeking a Staff Systems Engineer to architect, validate, and own the system-level behavior of a complex medical device ecosystem across the product lifecycle. You will define the end-to-end system architecture and translate user needs into testable...Medical device
$148.7k - $297.3k
...ResourcesIndustry: HealthcarePosted Date: 2026-09-01Abbott is a global healthcare leader that helps people live more fully at all... ...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000...Medical deviceWorldwide$120k - $140k
...development for kidney stone treatment. The ideal candidate will have a strong background in clinical engineering and experience in medical device testing. With a competitive salary range of $120,000 - $140,000, this role includes opportunities for growth, stock options,...Medical device- Getinge in Pleasanton, CA seeks an innovative engineer to lead early-stage concept generation and translational research for medical devices in a regulated environment. You will invent and develop novel technologies and advance them toward product development. The role...Medical device
- ...Systems Engineer to drive system-level verification for complex medical devices, spanning hardware, embedded software, mobile apps, wireless... ...plans, risk-based testing, and documentation to support regulatory submissions and product realization. Applicants should have...Medical device
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Global Regulatory Affairs Specialist - Medical Devices. Be the first to apply!
Related searches
- food regulatory Pleasanton, CA
- regulatory Pleasanton, CA
- regulatory engineer Pleasanton, CA
- regulatory contract Pleasanton, CA
- regulatory law Pleasanton, CA
- medical device Pleasanton, CA
- regulatory compliance Pleasanton, CA
- compliance team leader Pleasanton, CA
- corporate compliance Pleasanton, CA
- vendor compliance Pleasanton, CA