regulatory Jobs in San Francisco, CA

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Veeva Regulatory Information Management Database (RIM)

Dotsher Inc

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South San Francisco, California, USA

Contract

Role - Veeva Regulatory Information Management Database (RIM) 6+ months contract Location - South San Francisco, CA Start: ASAP Responsibilities include: Create standard operating process for Veeva naming conventions (Metadata) for regulatory documents.Create, assign, and manage Veeva workflows for regulatory documents as needed.Regulatory Operations trainer for Veeva-RIMTransfer current Module 3 Regulatory Documents from SharePoint into Veeva system.Assist with archiving documents from Health
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Posted 37 days ago | Updated 25 days ago

Manager, Consulting - Regulatory Research (IRB, CIP or CIM)

Kaiser Permanente

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Oakland, California, USA

Full-time

Description: Job Summary: Manages a team of consultants to ensure the alignment, buy-in, and coordination of diverse stakeholders to drive the implementation of successful business initiatives and projects. Managers the development and implementation of business initiatives, systems, and/or processes to a desired future state. Develops business strategy and ensures alignment and prioritization of organizational objectives and business initiatives. Manages complex projects or project components
Posted 36 days ago | Updated moments ago

Business Execution Consultant - Commercial Banking/Regulatory Reporting

Randstad Digital

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Concord, California, USA

Contract

job summary: Randstad Digital is hiring and we're looking for someone like YOU to join our team! If you are seeking a new opportunity, looking to grow in your career, or you know someone who is - we want to hear from you! Take a look at the below opportunity, or feel free to visit RandstadUSA.com to view and apply to any of our open roles. location: Concord, California job type: Contract salary: $89.06 - 94.06 per hour work hours: 8am to 5pm education: Bachelors responsibilities: - Act as a
Posted 18 days ago | Updated 1 hour ago

Regulatory Affairs

Judge Group, Inc.

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Palo Alto, California, USA

Full-time

Location: Palo Alto, CA Salary: $50.00 USD Hourly - $68.00 USD Hourly Description: Our client is currently seeking a Regulatory Affairs for a 12 month + contract. Hybrid position, 2 days in office (Palo Alto, CA). Position Description: *Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices according to regulatory requirements * Identifies, analyzes and implements country specific requirements necessary for product related submis
Posted 16 days ago | Updated 1 hour ago

Sr. Regulatory Affairs Specialist

APN Software Services, Inc

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Palo Alto, California, USA

Contract

Please contact Abdul on "" OR email me at "" *Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices according to regulatory requirements * Identifies, analyzes and implements country specific requirements necessary for product related submissions. *Recommend strategies for earliest possible approvals for marketing applications * Performs regulatory projects or acts as a member of the project steering group. * Submits required documentat
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Posted 16 days ago | Updated 1 day ago

Principal Regulatory Affairs Specialist (remote)

Medtronic

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Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w
Posted 1 day ago

CMC Regulatory Affairs Manager

TechSpace Solutions Inc.

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Remote

Third Party, Contract

Job Title : CMC Regulatory Affairs Manager Location : Remote Duration : 12 Months Responsibilities: Leading project teams, ensuring maintenance of team records and process-related documentation i.e., process maps, job aids, project trackers, checklists, etc.Responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance and defined regulatory strategies along with the preparation and review of information required for
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Posted 8 days ago | Updated 2 days ago

Senior Regulatory Affairs Specialist (Medical Devices)

ApTask

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Remote

Contract

Job Title: Senior Regulatory Affairs Specialist (Medical Devices) Location: Remote Duration: Long term contract Job Description: -Subject Matter Expert for Class II and Class 510(K) submission. -Hands on experience with 510(k) authoring, submissions, and communicating with the FDA. -Hands on experience with software as a Medical Device (SaMD) and validation requirements and applicable consensus standards. Key Responsibilities- -Authoring US FDA 510(k) submission using eSTAR submission tool.
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Posted 9 days ago

Principal Regulatory Affairs Specialist (Remote)

Medtronic

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Remote or Los Angeles, California, USA

Full-time

Careers that Change Lives Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's w
Posted 11 days ago | Updated 1 day ago

Project Manager - Credit Risk and Regulatory - Banking

V-Soft Consulting Group, Inc

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Remote

Contract

Project Manager - Credit Risk and Regulatory - Banking Primary Location: Chicago, Illinois V-Soft Consulting is currently hiring for a Project Manager - Credit Risk and Regulatory Banking for our premier client in Chicago, Illinois. WHAT YOULL NEED: Technical Requirements and Certifications PMI certification is preferred but not required. Education and Experience Bachelor's degree in Computer Science, Information Systems or Project Management is preferred 5+ years of experience as a Project Man
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Posted 12 days ago | Updated 1 day ago

Regulatory/ Pharmacovigilance Associate (REMOTE)

NetSource, Inc.

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Remote

Contract

Please note that this is a 1 year contract position. HIGHLIGHTED SKILLS: - Role can be 100% REMOTE - May travel for a possible mandatory meeting onsite (Raritan, NJ) for 1-2 days, not very often at all - Bachelors Degree required - Pharmacovigilance experience needed - Must be flexible / adaptive - Must be able to problem solve, and know when to ask for help - Working within the Global Environment / Global Teams - Regulatory Affairs experience - MAIN ASPECT OF ROLE: Support Aggregate Tracking p
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Posted 16 days ago | Updated 2 days ago

Technical Writer with ISO Compliance Regulatory experience

BayOne Solutions

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Remote

Contract

Technical Writer Location: Remote work Duration: 7 months Job description: We are seeking a Technical Writer to join our team and support the IT Operations project tracks within the ISO initiative. In this role, you will collaborate closely with the IT Ops project management team to conduct working sessions and engage with external stakeholders across various ISO tracks. The immediate focus of this position is to work collaboratively with the Infrastructure and Technology, IT Business Engagement