Regulatory Affairs Manager Jobs

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Regulatory Affairs Consultant

Stellar Consulting Solutions

Arkansas, USA

Full-time

Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly to match skill supply and demand on a real-time basis. Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and

Regulatory Affairs Project Manager - Structural Heart

Abbott Laboratories

Saint Paul, Minnesota, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future

Regulatory and Medical Affairs - Project Manager

Net2Source Inc.

Lawrence Township, New Jersey, USA

Contract

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap Right Talent Right Time Right Place Right Price and acting as a Career Coach to our consultants. Job Description: Onsite full time at Princeton Pike

Regulatory Affairs Specialist II (DePuy Synthes) - Medical Device Business Services, Inc.

Johnson & Johnson

Raynham, Massachusetts, USA

Full-time

Description DePuy Synthes, Inc. is currently recruiting for a Regulatory Affairs Specialist II to support Life Cycle Management and New Product Development. This role will work a Hybrid/Flex schedule with 3 days in office each week, located in Raynham, MA or West Chester, PA . About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatment

Regulatory Affairs Specialist I (Depuy Synthes/Spine) - Medical Device Business Services, Inc. (1 of 2)

Johnson & Johnson

Raynham, Massachusetts, USA

Full-time

Description DePuy Synthes, part of Johnson & Johnson MedTech, is recruiting for a Regulatory Affairs Specialist I to support our Spine business. This role is located on-site in Raynham, MA and will work a Flex/Hybrid schedule with three days of on-site and two days of off-site work . About Johnson & Johnson At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where tr

Senior Regulatory Affairs Specialist

Johnson & Johnson

Danvers, Massachusetts, USA

Full-time

Description Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. Remote work options may be considered on a case-by-case basis and if approved by the Company Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives. Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicia

Regulatory & Medical Affairs - Project Manager

Sunrise Systems, Inc.

Lawrence Township, New Jersey, USA

Contract

Job Title: Regulatory & Medical Affairs - Project Manager Job ID: 24-01565 Location: Lawrence Township, NJ, 08648 Duration: 06 Months contract on W2 Onsite full time at Princeton Pike. Innovation and Digital Health, Project Manager - Digital Optimization Initiatives Position Summary The Innovation Lab team partners with R&D stakeholders to design and deliver innovative analytics solutions that help them make better decisions, reduce costs and/or drive efficiencies. Our diverse analytics team of

Regulatory Affairs Senior Manager

Software Guidance & Assistance

Hawthorne, New York, USA

Full-time

Software Guidance & Assistance, Inc., (SGA), is searching for a Regulatory Affairs Senior Manager for a FULL TIME assignment with one of our premier Pharmaceutical Services clients in Hawthorne, NY. Responsibilities: US Agent for all Firm's products, responsible for communication between the FDA and manufacturing sites. Communicate and follow-up status with FDA for any Chemistry, Bioequivalence and Patents issues and correspondences on both pending and approved applications Lead, guide and t

Manager, Product Management- External Affairs

Capital One

McLean, Texas, USA

Full-time

Center 2 (19050), United States of America, McLean, Virginia Manager, Product Management- External Affairs External Affairs (EA) works with external and internal stakeholders to create a world of greater socioeconomic opportunity through advocating for an inclusive society, building thriving communities, and creating financial tools that enrich lives. Our teams include Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, Government and Politica

Technical Project and Budget Manager (Veterans Affairs)

LTS

Remote

Full-time

LTS is seeking a Technical Project & Budget Manager to support the Department of Veterans Affairs (VA). The Technical Project & Budget Managers primary responsibilities will be to provide strategic support through implementing SAFe Agile Framework practices/principles, while also managing the overall Sub-Product Line budget. This position is 100% remote. LTS provides trusted consulting, and solutions in an increasingly complex and growing world. Our deep expertise in technology and analytics hel

Public Affairs Specialist- (Joint Information Center Manager)

FEMA

Full-time

Summary The Joint Information Center Manager (JIMG) position develops, updates, and maintains the function plan for the Joint Information Center component of External Affairs and oversees its implementation. A JIMG is responsible for serving as a FEMA spokesperson for print, television, radio and social media as well as supervising assigned subordinates. Duties What will I do in this position if hired? In this Public Affairs Specialist- (Joint Information Center Manager) position, you will dev

Software Engineering Senior Manager(Global Regulatory Reporting)

Wells Fargo

New York, New York, USA

Full-time

About this role: Wells Fargo is seeking a Engineering Senior Manager (Global Regulatory Reporting) as part of the Wholesale Operations Technology (WOT) Organization. This role will be accountable for the Wells Fargo Global Transaction Reporting ecosystem and will work closely with the Regulatory Reporting Product owner and team. This role will oversee the work to support three global regions (Americas, EMEA and APAC). Critical to this role will be a strong understanding of OTC products and thei

IT Security Manager(Risk and Regulatory)(only W2)

Intellibee Inc

Detroit, Michigan, USA

Full-time

IT Security Manager Top Skills: ** Exceptional understanding of Risk and Regulatory requirements in Financial Services industry; ** Exceptional written and verbal communication skills. Ability to interact across multiple organizations and levels; ability to mentor and coach team members; ** Several years of experience in Quality Assurance/Quality Control, IT Risk Management, and Information Security ability to evaluate and design effective controls; ** Knowledge and experience in performing ass

Regulatory Affairs Project Leader

Intellectt INC

Plymouth, Minnesota, USA

Contract

Hello, This is Venkat from Intellectt Inc. Please find the below position and let me know your response. Title: Regulatory Affairs Project Leader Location: Plymouth, MN Duration: 12+ Months Job Description: This individual will support global Regulatory changes with responsibility for monitoring, analyzing, interpreting, and communicating medical device regulations to a broad audience. Daily, this individual will work with regional experts to understand the regulation change and determine