Regulatory Affairs Manager jobs

Princeton, New Jersey

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Today

Position: Regulatory & Clinical Affairs Manager Location: Princeton, NJ Onsite (open to Relocating) Type: Permanent / Direct Hire / Full Time Primary Responsibilities: Preparation and execution of regulatory submissions, including FDA 510(k) submissions, software modifications, and international registrations as applicable.Assess regulatory impact of software, AI/ML, cybersecurity, and product changes.Develop regulatory strategies and recommendations for new products and software upgrades.Suppo

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Full-time

Depends on Experience

Global Regulatory Affairs and Compliance Manager- Medical Devices

Albuquerque, New Mexico

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Today

How will you make an impact?The Regulatory Affairs & Compliance Manager is responsible for developing, implementing, and maintaining regulatory affairs and quality system compliance programs to ensure continued compliance with applicable global regulations, standards, internal and customer requirements. This position provides regulatory affairs leadership and compliance oversight across manufacturing operations, supports regulatory inspections and external audits, and partners with cross-functio

Full-time

Sr Manager of Regulatory Affairs

Canyon Lake, Texas

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Senior Manager, Regulatory Affairs for a Full Time assignment with one of our premier Utilities clients in Texas . Responsibilities : Lead regulatory affairs activities for a regulated utility operation, ensuring alignment between business objectives, financial performance, and regulatory requirements. Develop and execute rate case strategies, including preparation of regulatory filings, supporting schedules, and testimony for stat

Full-time

Project Manager, Regulatory Affairs (Clinical and CMC)

Remote

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13d ago

Title: Project Manager, Regulatory Affairs (Clinical and CMC) Location: Remote Employment Type: Contract Compensation: Pay Range:$49.00-$70.00 Per Hr Job Summary: This is a remote contract position focused on managing regulatory affairs projects related to clinical and CMC processes. The role involves implementing a chromatography data system, ensuring compliance with regulations, and collaborating with various stakeholders. A strong understanding of life sciences and regulatory principles is

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Contract, Third Party

$49 - $70

Regulatory Affairs Specialist

San Francisco, California

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7d ago

About Nexinfo NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. We offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. We aims to help businesses across industries achieve their goals through industry best practices, lean process design and advanced software solutions. Our ERP-related services address challenges such as invent

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Third Party, Contract

$60 - $70

Global Regulatory Affairs Specialist

Irvine, California

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Today

Take your regulatory affairs expertise to the next level with an opportunity to support innovative diagnostic products on a global scale. This role offers the chance to work with cross-functional teams, contribute to international regulatory submissions, and play a key role in bringing compliant healthcare solutions to markets around the world. Location: Irvine, CA (Hybrid) Pay Rate:$55 - $60/hr Employment Type: 6-Month Temporary Assignment (Projected through March 1, 2027) Schedule: Monday-F

Full-time

Compensation information provided in the description

Regulatory Affairs Data Coordinator

Remote or Irvine, California

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Today

Kelly Science and Clinical FSP is currently seeking an RA Data Coordinator for a long-term engagement in Irvine, CA with one of our Global clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eli

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Contract

Regulatory Research Associate

Menlo Park, California

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2d ago

Position: Regulatory Research Associate Location: Menlo Park, CA 94025 Duration: Full Time About the Role We are seeking a proactive and intellectually curious Regulatory Research Associate to support regulatory strategy, compliance activities, and market intelligence for innovative wearable healthcare and wellness devices. This individual will help navigate a rapidly evolving regulatory landscape while supporting product development, submissions, and compliance initiatives across global marke

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Full-time

80,000 - 90,000

Regulatory Advisory and Optimization Analyst, Officer, Onsite

Boston, Massachusetts

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21d ago

Who we are looking for The Regulatory Advisory and Optimization team is responsible for staying ahead of regulatory affairs and changes impacting SSM businesses. The team actively participates in industry conferences and forums, monitors market and regulatory developments, meets with clients, and analyzes competitors to provide strategic guidance. Additionally, the team identifies and explores regulatory optimization opportunities through innovative structures such as Significant Risk Transfers

Full-time

USD 70,000.00 - 118,750.00 per year

Regulatory Affairs Specialist

New Jersey

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Today

IKCON TECHNOLOGIES INC delivers exceptional IT services and solutions that provide clients with definite edge over competitors and promoting highest standards of quality. We are currently looking for a Regulatory Affairs Specialist with one of our clients in Remote, Remote. If you are actively looking for opportunities, please send us your updated resume with your contact details. JOB TITLE Regulatory Affairs Specialist/Senior Specialist for Drug-Device Combination Products CITY Remote STATE

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Contract, Third Party