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National Program Manager - Regulatory

DISH

Walnut Creek, California, USA

Full-time

Company Summary DISH, an EchoStar Company, has been reimagining the future of connectivity for more than 40 years. Our business reach spans satellite television service, live-streaming and on-demand programming, smart home installation services, mobile plans and products, and now we are building America's First Smart Network . Today, our brands include EchoStar, Hughes, DISH TV, Sling TV, Boost Infinite, Boost Mobile, DISH Wireless, OnTech and GenMobile. Department Summary Surpassing network

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

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

Regulatory Affairs Specialist, Cell & Gene Therapy

Zachary Piper Solutions, LLC

Philadelphia, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies. Responsibilities of the Regulatory Affairs Specialist, Cell & Gene Therapy Coordinate and manage timing for regulatory submissions, collaborating with internal teams and stakeholders. Oversee external publishing coordination for IND/CTA submissions and related documents.

Regulatory Affairs Professional

Cygnus Professionals

Palo Alto, California, USA

Contract

Knowledge: Deep professional know-how and experience in one Sub Job Family. Masters domain. Transfers and applies know-how to / in various contexts. Solid professional judgment and problem solving competence. Improves existing processes and approaches Product Registration Experience: Experience with FDA 510(k) applications, Health Canada license applications and EU MDR technical filesKnowledge of regulatory guidance documents and requirements for product classification determination, FDA 510(k)

Sr. Regulatory Operations Specialist

Zachary Piper Solutions, LLC

Philadelphia, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a Sr. Regulatory Operations Specialist to support a growing and innovative cell and gene therapy company in Philadelphia, PA (Hybrid Schedule). Responsibilities for the Sr. Regulatory Operations Specialist Coordinate diverse regulatory submissions by collaborating with internal teams and stakeholders, and develop content plans for IND & CTA dossiers. Lead interactions with external publishing teams to compile IND or CTA submissions, including reports and

Regulatory Affairs

Judge Group, Inc.

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

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

Regulatory Life Sciences Managing Consultant

Navigant Consulting

McLean, Virginia, USA

Full-time

Job Family : Strategy & Transformation Consulting Travel Required : Up to 10% Clearance Required : Ability to Obtain Public Trust What You Will Do : Is life sciences in your DNA? Breakthroughs in pharma are helping people live longer, healthier lives while bringing hope to patients with rare diseases. With outpaced growth across the industry and advancements in drug development this is undoubtedly a transformative time for regulators, developers, and patients. Guidehouse's Regulatory Life Scien

Sr. Regulatory Affairs Specialist

APN Software Services, Inc

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

Regulatory and Client relationship management

Net2Source Inc.

New Jersey, USA

Full-time

Role: Regulatory and Client relationship management Work Location: New Jersey Or Chicago, IL Hire Type: Fulltime 1.The candidate should be Assertive, 2.Situational Leadership, 3.Process Mapping Competency 4.RAPS (or equivalent) Certification is nice to have 5.1 2 years of business development and client relationship management desirables Experience in 2-3 additional LS specific domain areas would be desirable "Plan and Execute Regulatory Transformation project with excellent presentation skills,

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 Life Sciences Senior Consultant

Navigant Consulting

McLean, Virginia, USA

Full-time

Job Family : Strategy & Transformation Consulting Travel Required : Up to 10% Clearance Required : Ability to Obtain Public Trust What You Will Do : Is life sciences in your DNA? Breakthroughs in pharma are helping people live longer, healthier lives while bringing hope to patients with rare diseases. With outpaced growth across the industry and advancements in drug development this is undoubtedly a transformative time for regulators, developers, and patients. Guidehouse's Regulatory Life Scien

Regulatory Life Sciences Associate Director

Navigant Consulting

McLean, Virginia, USA

Full-time

Job Family : Strategy & Transformation Consulting Travel Required : Up to 10% Clearance Required : Ability to Obtain Public Trust What You Will Do : Is life sciences in your DNA? Breakthroughs in pharma are helping people live longer, healthier lives while bringing hope to patients with rare diseases. With outpaced growth across the industry and advancements in drug development this is undoubtedly a transformative time for regulators, developers, and patients. Guidehouse's Regulatory Life Scien

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.

Liquidity Regulatory Reporting Manager

Intraedge

New York, New York, USA

Contract

Liquidity Regulatory Reporting Analyst/Manager Location: NYC, NY (Onsite position / No Remote work) Longterm contract As a Liquidity Manager specializing in LCR, 2052a, NSFR, Governance, and Controls. Nice to have: Extensive expertise in leveraging tools such as Axiom, Tableau, and SQL to ensure financial institutions maintain optimal liquidity positions while adhering to regulatory requirements.

Program Manager (Liquidity /Regulatory Reporting)

Intraedge

New York, New York, USA

Contract

Liquidity Reporting Manager Location: NYC, NY (Onsite position / No Remote work) Longterm contract Required Skills: Deep understanding of Liquidity Coverage Ratio (LCR), 2052a, Net Stable Funding Ratio (NSFR), and governance frameworks. Generate/Produce daily consolidated FR 2052a results

Engineer, Sr/Principle Regulatory - EN

Constellation Energy

Kennett Square, Pennsylvania, USA

Full-time

COMPANY OVERVIEW As the nation's largest producer of clean, carbon-free energy, Constellation is a company purposely-built to meet the challenges of the climate crisis. Constellation has been the leader in clean energy production for more than a decade and we are growing our company and capabilities. Now, we're accelerating, speeding our low-carbon or no-carbon power to more people in more places, day and night, providing our customers and communities with options to buy, manage and use energy

Regulatory Affairs Associate

Apex Systems

Mountain View, California, USA

Full-time

Job#: 2027155 Job Description: Client: IRIDEX Position: Regulatory Affairs Associate Location: Mountain View, CA Estimated Duration: The client approximates that this project may last up to 5 months. However, there is no guarantee of employment for any length of time. Pay Rate Range: $35 - $45/hr IRIDEX Corporation is a medical device manufacturer and operates in a global regulated environment (e.g. FDA). Regulations include (but are not limited to) FDA 21 CFR 820, EN ISO 13485, Health Cana