MedTech Project Coordinator for Regulatory Submissions
Intuitive Surgical, Inc.
Intuitive Surgical, Inc. is looking for a Project Coordinator to support cross-functional product development programs in Sunnyvale, California. You will coordinate activities across various subsystems, ensuring timely execution and operational efficiency. The ideal candidate will have at least 3 years of experience in project coordination, a Bachelor's degree, and proficiency in tools like Microsoft Project and JIRA. This role is completely onsite. #J-18808-Ljbffr Intuitive Surgical, Inc.
- ...Description Primary Function of Position: The Project Coordinator will support complex, cross‑... ..., and Clinical, with a focus on regulatory and clinical readiness. The coordinator... ...such as V&V deliverables and regulatory submissions. Job Requirements Work with Program...RegulatoryLocal area
- Job Overview The Project Coordinator will support complex, cross‑functional product development... ..., and Clinical, with a focus on regulatory and clinical readiness. The coordinator... ...validation deliverables and regulatory submissions. Responsibilities Track project plans...RegulatoryLocal areaShift work
$90k - $180k
Abbott Laboratories is seeking a Senior Regulatory Affairs Specialist at their Santa Clara, CA location. This role involves supporting... ...regulatory input for product lifecycles and handling submissions to regulatory authorities. The ideal candidate should have a...Regulatory- Intuitive is seeking a Project Coordinator in Sunnyvale, California to support complex product development programs across various subsystems... ...facilitating operational efficiency and compliance with regulatory standards. The ideal candidate should have a Bachelor's Degree...Regulatory
- ...knowledge of electronic security systems and project management experience within a physical... ..., including mobilization, design coordination, installation, commissioning, and security... ...Expertise Anticipates business, regulatory, and operational risks within security...RegulatoryWork experience placementWork at office
$71.9k - $94.58k
...shape a brighter way forward. What this job involves The Project Coordinator - Lab Moves at JLL is responsible for supporting the planning... ...Knowledge of laboratory safety guidelines, protocols, and regulatory requirements is preferred. This position does not provide...RegulatoryDaily paidLocal areaRelocation$35 - $40 per hour
The Project Coordinator provides overall administrative support to project teams for day-to-day activities. Provides overall administrative... ...Best Practices. Works with the project team to ensure all regulatory compliances are met including insurance and preliminary...RegulatoryPermanent employmentTemporary workWork experience placementFor subcontractorWork at office- ...Responsibilities Review and intake physical security project assessments from business stakeholders.... ...project workflow: mobilization, design coordination, installation, commissioning, and... ...platforms. Anticipates business, regulatory, and operational risks within security...RegulatoryWork experience placementWork at office
- 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...Regulatory
- ...Mechanical Engineer in the Medical Device / MedTech industry Strong experience designing... ...teams including R&D, Quality, Regulatory, Manufacturing, and Suppliers Support verification... ...medical devices Experience with FDA submissions, DHF (Design History File), DMR...Regulatory
$43.77 - $56.9 per hour
...Stanford Health Care. Responsibilities Plan, coordinate, and participate in the implementation... ...to inquiries. Manage access to hospital regulatory and compliance software, and manage the... ...support experience, focusing on project coordination, budget preparation, monitoring...RegulatoryHourly payWork at office$43.77 - $56.9 per hour
Overview Plans, coordinates, and participates in the performance of varied and responsible work in the administration, project administration, and operation of specialized programs or projects... ...materials. Manage access to hospital regulatory and compliance software, implement...RegulatoryHourly payWork at office- ...The Senior Regulatory Affairs Specialist leads regulatory operations activities... ...across multiple franchises. Coordinate and align inputs from cross-... ..., or international regulatory submissions. Experience managing complex cross-functional projects and deliverables. Knowledge of...Regulatory
- ...We are searching for an experienced regulatory professional to work within the Companion... ...with a history of successful regulatory submissions, registrations, 510(k)’s, and PMA approvals... ...will represent Regulatory Affairs on project teams and in close collaboration with...Regulatory
- Creative Solutions Services, LLC in Sunnyvale, CA is seeking a Sr. Regulatory Affairs professional with over 8 years of experience in... ...devices. This role involves developing regulatory plans, preparing submissions, and ensuring compliance with U.S. and Canadian regulations....Regulatory
- ...This role is remote. The Project Control Analyst provides... ...This role supports onboarding coordination, security clearance processing... ...- Support preparation and submission of contractual deliverables... ...compensation. Maximus will comply with regulatory minimum wage rates and...RegulatoryMinimum wageFull timeContract workTemporary workWork experience placementRemote work
- Abbott is hiring a Regulatory Affairs Specialist for their Vascular Division in Santa Clara... ...should possess strong analytical, project management, and communication skills, along... ...regulatory strategies and preparing submissions, contributing significantly to product...Regulatory
- ...at The Foundry, an acclaimed medtech venture incubator, funded by... .... Apreo is seeking a Regulatory Affairs Specialist to support... ...and execution of regulatory submissions for medical device products,... ...deliverables for new products or projects. Support Q-submissions (e.g....RegulatoryCasual workRemote workRelocationRelocation package
- ...for compliance with national/regional/global regulations. Regulatory support for integration activities including reviews of... ...with regulations. Prepares document packages for regulatory submissions for new and mature products to ensure alignment and compliance...RegulatoryApprenticeshipLocal area
- ...in Santa Clara, CA. The role requires ensuring compliance with regulatory standards for medical devices. Responsibilities include... ...communication and data analysis skills. Competitive compensation and substantial benefits are offered. #J-18808-Ljbffr Johnson & Johnson MedTechRegulatory
- ...Title: Regulatory Affairs Associate Location: Santa Clara, CA Duration: 12Months 100% Onsite Summary: We are looking for an experienced Regulatory Affairs professional to manage regulatory submissions and approvals for medical devices, including high-risk (Class III) implantable...RegulatoryTemporary workFlexible hours
- ...practical compliance solutions, manage regulatory requirements, and support business objectives... ...reviews and BIS license application submissions. Maintain export compliance records and... ...export compliance initiatives and projects across the organization. Qualifications...RegulatoryWork at office
- ...Monitor clinical outcomes and patient safety standards Support implementation of best practice care models Maintain compliance with regulatory standards Quality & Compliance Ensure compliance with Joint Commission, state, and federal regulations Lead quality...RegulatoryFull timeMonday to FridayShift workDay shift
$30 per hour
...Clinical Liaison Coordinator / LVN Position Type: Full-Time Schedule: Monday – Friday, 9:... ...intake to placement quickly while ensuring regulatory compliance and member safety. Job... ...timely communication and documentation submission to MCPs 4. Field Liaison & Relationship...RegulatoryFull timeImmediate startRemote workMonday to Friday- A global healthcare leader is seeking a Regulatory Affairs Associate in Santa Clara, CA. This role involves managing regulatory submissions and approvals for medical devices, particularly Class III products. Candidates should have a Bachelor's or Master's degree in a relevant...Regulatory
- Job Title: Sr. Regulatory Affairs Location: Sunnyvale, CA - Hybrid... ...changes, preparing regulatory submissions, maintaining regulatory... ...with minimal supervision. Coordinate with technical experts to provide... ...guidance and regulatory input to projects and issues, ensuring cross-...Regulatory3 days per week
$109k - $175k
Johnson & Johnson MedTech is seeking a Senior Post Market Surveillance Specialist in Santa Clara, California. This role involves managing complaint records, regulatory reporting to the FDA, and participating in audits. The ideal candidate has over 5 years of experience...Regulatory- A leading staffing company is seeking an experienced regulatory professional for their Companion Diagnostics team. The ideal candidate... ...experience in IVDs and medical devices, leading successful submissions and working directly with regulatory bodies like the FDA. Responsibilities...Regulatory
$28 - $40 per hour
...Contracts Department. The primary area of responsibility of the project coordinator will be to act as liaison between internal and external... ...submit, and maintain compliance with all project labor and regulatory requirements for private and public works projects,...RegulatoryHourly payContract workWork at officeLocal area$26.5 - $59 per hour
Regulatory Intern Location: Santa Clara, California, United States of America Term June to... ...procedures to assist in regulatory research, project publishing, organization, and... ...products. Gain and apply knowledge of submission structures and technical requirements for...RegulatoryHourly payFull timeInternshipWork at officeLocal area
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