regulatory Jobs in Seattle, WA

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General Manager, Regulatory Governance

Microsoft Corporation

Redmond, Washington, USA

Full-time

$desc Qualifications Required/Minimum Qualifications: Bachelor's Degree AND 10+ years work experience in product compliance or governance, program management, process management, process improvementOR equivalent experience.8+ years people management experience and managing cross-functional and/or cross-team projects Additional or Preferred Qualifications : Broad business and/or regulatory background Ability to navigate engineering organizations Understanding of external regulations and the r

Senior Corporate Counsel, Enterprise Cloud Services Regulatory Oversight

Microsoft Corporation

Redmond, Washington, USA

Full-time

$desc Qualifications Required/Minimum Qualifications Juris Doctorate Degree or Equivalent International DegreeOR Completion of a Legal Apprenticeship.Active license to practice law in a jurisdiction and capable of meeting admission requirements in relevant jurisdiction.7+ years experience as a practicing attorneyOR equivalent practice of law.Experience counseling engineering or other technical clients and translating legal requirements into actionable engineering-facing guidance Preferred Qual

Research Intern - Scientific & Regulatory Affairs - Health Futures

Microsoft Corporation

Redmond, Washington, USA

Full-time

$desc Qualifications Required Qualifications Enrolled in a Masters, PhD, or Graduate program related to digital health policy, regulation, user research and/or bioethics. At least 1 year of experience in a healthcare or life sciences R&D or policy setting. Other Requirements Research Interns are expected to be physically located in their manager's Microsoft worksite location for the duration of their internship. In addition to the qualifications below, you'll need to submit a minimum of two r

SAP PRA Consultant (Regulatory Reporting)

Activesoft, Inc.

Remote

Contract

SAP PRA Consultant (Regulatory Reporting ) Occasional Travel to Houston TX (Argentina, Brazil) Job Description: 1) Revenue Accounting and Disbursement 2) Production Accounting :Gas Booking and contracting, allocation, Well level accounting for production 3) Regulatory Reporting govt and federal agency including annual reporting.

Regulatory Affairs Specialist III

Fusion Life Sciences

Remote

Contract

Job Title: Regulatory Affairs Specialist (Remote) Summary: Seeking a fluent French speaker to guide EU MDR project teams. Responsible for preparing and submitting EU MDR documentation for medical devices (Class , IIa, IIb, I sterile or reusable) for CE marking and EU commercial release. Collaborate with cross-functional teams and Notified Bodies. Supervision: Reports to Sr. Manager or Director of Regulatory Affairs. No supervisory responsibilities. Essential Duties: Ensure EU MDR compliance for

SAP Revenue / Production Accounting & Regulatory Reporting Consultant (PRA)

Activesoft, Inc.

Remote

Contract

SAP Revenue/Production Accounting/Regulatory Reporting Consultant (Oil & Gas) Location: Houston, TX/Argentina/Brazil (for workshops)+ (Travel expenses) Duration: ASAP to 12/13/2024 with the possibility of an extension Job Description: 1) Revenue Accounting and Disbursement 2) Production Accounting :Gas Booking and contracting, allocation, Well level accounting for production 3) Regulatory Reporting govt and federal agency including annual reporting.

Regulatory/ Pharmacovigilance Associate (REMOTE)

NetSource, Inc.

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

Senior Regulatory Affairs Specialist (Medical Devices)

ApTask

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.

Technical Writer with ISO Compliance Regulatory experience

BayOne Solutions

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