Medical Devices Project Coordinator — Regulatory Readiness
Intuitive
Intuitive is seeking a Project Coordinator in Sunnyvale, California to support complex product development programs across various subsystems. This role is crucial for ensuring timely execution of deliverables while facilitating operational efficiency and compliance with regulatory standards. The ideal candidate should have a Bachelor's Degree and 3+ years of project coordination experience, along with strong communication skills and proficiency in project management tools such as JIRA and Excel. #J-18808-Ljbffr Intuitive
- jobr.pro in Sunnyvale, California is looking for a Project Coordinator to support complex product development programs within Advanced Engineering. The role involves ensuring timely execution of deliverables across various subsystems and facilitating governance. The ideal...RegulatoryMedical device
- Job Description The Project Coordinator will support complex, cross-functional... ..., with a focus on regulatory and clinical readiness. The coordinator will... ...execution including supporting device shipments to clinical... ...documentation in accordance to medical device design control...RegulatoryMedical deviceLocal areaFlexible hoursShift work
- ...professional to provide compliance support to the Regulatory Affairs organization. The ideal... ...Quality Systems, hands-on exposure to medical device regulations, and a strong ability to... ...role is critical for maintaining regulatory readiness. #J-18808-Ljbffr The Fountain GroupRegulatoryMedical device
- ...provide compliance support to the Regulatory Affairs organization by:... .... Participating in RA projects. Qualifications: Degree with... ...experience. Hands‑on exposure to medical device regulations (US FDA, CE),... ...implement mitigations and sustain regulatory readiness. #J-18808-Ljbffr...RegulatoryMedical device
- ...manage end-to-end testing activities for medical device software (embedded + system level).... ...Collaborate with R&D, systems engineering, regulatory, and quality teams. Oversee test case... ...estimations, sprint planning, and release readiness. Conduct peer reviews of technical and...RegulatoryMedical device
- ...live more active, healthier lives. Be ready to make something great when you come here... ...Lead Auditor to support regulated medical device features. If you are passionate about the... ...supplier audit program to ensure ongoing regulatory compliance and encourage continuous...RegulatoryMedical device
- ...support clinical trial reporting, regulatory submissions, and publications... ...cleaning, interim analyses, medical review, and final study... ...documentation to support audit readiness and collaborative programming... ...pharmaceutical, biotechnology, or medical device industry. Candidate is a...RegulatoryMedical deviceInterim role
$25 per hour
...This role supports quality and regulatory compliance activities within a medical device manufacturing environment. The Compliance... ..., training records, and audit readiness Assist with internal and... ...reporting and metrics tracking Coordinate training activities and monitor...RegulatoryMedical deviceContract workFor contractorsWork at officeLocal area$146.3k - $244.1k
...live more active, healthier lives. Be ready to make something great when you come here... ...Lead Auditor to support regulated medical device features. If you are passionate about the... ...supplier audit program to ensure ongoing regulatory compliance and encourage continuous...RegulatoryMedical deviceRelocation- ...Compliance About the Company Global medical device company ensuring compliant cross-border... ...supporting uninterrupted patient care, regulatory approvals, and global commercial... ...for driving automation to improve audit readiness and reduce clearance delays, and must have...RegulatoryMedical device
- ...support clinical trial reporting, regulatory submissions, and publications... ...cleaning, interim analyses, medical review, and final study... ...documentation to support audit readiness and collaborative programming... ...pharmaceutical, biotechnology, or medical device industry. Candidate is a...RegulatoryMedical deviceInterim role
- ...build scalable, future-ready digital platforms that drive... ...and risk management in medical device development, and solid... ...schedule, cost, quality, and regulatory requirements. Act as... .... Mentor and coach project managers and program coordinators on program management best...RegulatoryMedical deviceContract work
- ...in protecting the validated state of medical devices, enabling safe and timely product launches... ...capability, quality performance, and regulatory compliance. Lead or support CAPA and... ...manufacturing capacity, scalability, and tooling readiness to support volume ramps without...RegulatoryMedical device
- ...a life. If you're ready to contribute to something... ..., NPI or Sustaining projects to manage. Expected... ..., and identify and coordinate issue resolution and... ...the Pharmaceutical or Medical Device industry (or similar... ...knowledge of ISO and regulatory restrictions. Additional...RegulatoryMedical deviceLocal areaWorldwideFlexible hours
$130 - $140 per hour
Director of Regulatory Affairs, Business Excellence 1... ...through process design, project oversight, and... ...execution of action items in coordination with the RegLT.... ...with audit/inspection readiness and regulatory documentation... ...Industry, Medical Device Industry, Regulatory...RegulatoryMedical deviceContract workRemote work$163k - $237k
...following industries: medical devices, consumer goods/... ..., multi‑disciplinary projects from start to finish.... ...specifications that include regulatory safety requirements... ...influence and ensure readiness for new and upcoming... ...others. You will require coordination with multiple cross‑...RegulatoryMedical deviceFull time$100k
...Clinical Specialist for Shockwave Medical, Inc. located in West... ...more personalized treatments. Ready to join a team that's pioneering... ...standard of care for medical device treatment of atherosclerotic... ...Clinical Practice (GCP) and regulatory compliance guidelines for clinical...RegulatoryMedical deviceLocal areaRemote work$50 - $60 per hour
...primarily focusing on software and medical device projects rather than pharmaceuticals... .... Track and maintain regulatory documentation and ensure... ...delinquencies in a timely manner, coordinating with internal teams and... ..., properly uploaded, and ready for submission, coordinating...RegulatoryMedical deviceHourly payContract workTemporary workFlexible hours- ...Product Development team focused on robotic-assisted platforms in China. This role involves collaborating with design teams and regulatory bodies to ensure successful product launch and compliance. The candidate will be responsible for technical contributions to the product...RegulatoryMedical device
- ...in Sunnyvale, CA to champion user-centered design and lead usability projects. This role will integrate human factors principles across product development to enhance usability, safety, and regulatory compliance. Candidates should have a background in Human Factors Engineering...RegulatoryMedical device
$165k - $180k
...point of care breast imaging device that allows high quality breast... ...into a cohesive, production‑ready software product. Architect... ...side processing, aligning with regulatory requirements. Build and... ...integration. Experience with medical device software development and...RegulatoryMedical deviceRemote workWorldwide- ...potential to change a life. If you're ready to contribute to something bigger than... ...security for network-connected medical devices as well as cloud security for web applications... ..., and incident response. Support regulatory and industry security requirements relevant...RegulatoryMedical deviceLocal areaWorldwideFlexible hours
- ...change a life. If you're ready to contribute to something bigger... ...research, engineering, regulatory, and clinical teams to develop... ..., validated, and scalable medical device software. The ideal candidate... ...Independently lead projects to conceive, develop, and implement...RegulatoryMedical deviceWork at officeLocal areaWorldwideFlexible hours
- ...change a life. If you're ready to contribute to... ...and managing a diverse project portfolio to ensure that... ...highest standards for regulatory submissions and scientific... ...journals, and medical conferences. Explore novel... ...trials, surgical medical device clinical research strongly...RegulatoryMedical deviceLocal areaWorldwideRelocationFlexible hours
- .... You will define manufacturing KPIs, lead scale-up operations, and ensure compliance with regulatory standards. The ideal candidate has 5+ years of experience in medical device manufacturing, a strong foundation in design and assembly of electromechanical systems, and...RegulatoryMedical device
$35 - $40 per hour
...junior team members, coordinates work with vendors and... ...to support facility projects and specialized work.... ...applicable building codes and regulatory requirements relevant... ...and parts to ensure readiness for maintenance and... ...a manufacturing or medical device environment is...RegulatoryMedical deviceWeekly payPermanent employmentContract workTemporary workFor contractorsMonday to FridayDay shift$214k - $356.6k
Apple Inc. in Cupertino, California is seeking an International Regulatory Affairs Lead for their Health group. This leadership role involves guiding regulatory strategies for medical device features globally and collaborating with cross-functional teams to navigate complex...RegulatoryMedical device$75 - $80 per hour
Technical Project Manager - QMS Transformation Santa... ...validation, audit readiness, and supporting change... ...across IT, Quality, Regulatory, Engineering, Operations... ..., and performance Coordinate across internal and... ...ComplianceQuest) preferred Medical device, MedTech, or...RegulatoryMedical deviceLong term contractLocal area3 days per week- ...change a life. If you’re ready to contribute to... ...to Manger/Sr. Manager, Medical Sciences and requires... ...product development, regulatory, post‑market surveillance... ...therapeutic areas, competitor devices, current clinical/... ...utilizing appropriate project management tools....RegulatoryMedical deviceLocal areaWorldwideShift work
- ...We are searching for an experienced regulatory professional to work within the Companion... ...regulatory experience working in IVD, Medical Devices, or Pharmaceuticals, with a history of... ...and will represent Regulatory Affairs on project teams and in close collaboration with pharmaceutical...RegulatoryMedical device
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