Regulatory Affairs jobs

San Francisco, California

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25d ago

Title: Director, Regulatory Affairs Location: San Francisco Bay Area (Onsite) Job Description: Reports into Regulatory Affairs, Global Filing & Registration: High-Impact position to lead cross-functional development & regulatory submission activities for registrational oncology programs in the US.Collaborate closely with Program Teams and Global Regulatory Leads to advance effective & consistent regulatory strategies to enable successful filing of approval of New Drug Applications.Develop strate

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Contract

$90 - $100

Regulatory Affairs Specialist

Remote

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9d 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

Regulatory & Clinical Affairs Manager

Princeton, New Jersey

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9d ago

Role: Regulatory & Clinical Affairs Manager Locations : Princeton, NJ (Onsite) (Full Time /Permanent) Note* FULLTIME Role and This role is on-site at Princeton, NJ The Role The Regulatory & Clinical Affairs Manager will play a key role in supporting the Company s regulatory and clinical initiatives across product development, regulatory submissions, and hospital collaborations. This position is intended for a motivated professional seeking to grow into increasing levels of responsibility withi

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Full-time

$160,000 - $170,000

CMC Regulatory Affairs Consultant

Wilmington, Delaware

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5d ago

CMC Regulatory Affairs ConsultantJob Type: Contract 12 Months Location: Wilmington, DE Hybrid/Onsite Work Arrangement: 3 Days Onsite per Week Non-Negotiable Required QualificationsBachelor''s degree or higher in Pharmacy, Chemistry, Biology, Life Sciences, Pharmaceutical Sciences, or a related scientific discipline.Strong hands-on experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry.Experience supporting large molecules and/or small molecules.Experience wit

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Contract, Third Party

Depends on Experience

Regulatory Affairs Specialist

Lake Forest, California

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11d ago

Job title: Regulatory Affairs Strategy Associate Location: Lake Forest, CA Duration: Permanent The Regulatory Affairs Strategy Associate, reporting to the Senior Director of Regulatory Affairs (LLSI), is primarily responsible for the regulatory strategy, ensuring local product registration and facilitating health registration approvals. WHAT YOULL BRING : Bachelors Degree or Equivalent years of directly related experience (or high school +7 yrs; Assoc.+5 yrs; M.S.+3 yrs) 7 Years of Relevant E

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Full-time, Third Party

Depends on Experience

Regulatory Affairs Specialist 4

Sunnyvale, California

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2d ago

Primary Function of Position The Sr. Regulatory Affairs primary responsibilities include developing regulatory plans, reviewing design input/output documentation, identification of applicable standards and guidance documents, performing regulatory assessments to determine the impact of design/process changes, preparing regulatory submissions, maintaining regulatory filings and licenses. Essential Job Duties Provide regulatory guidance to product teams, develop regulatory plans, a

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Third Party, Contract

$60 - $60

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 Specialist

Remote

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2d ago

Job Title:Regulatory Specialist Location:Rosemont, IL - Remote Duration: Long Term Contract Key Responsibilities: Provide strategic input and technical guidance on regulatory requirements to R&D project teams. Develop and implement regulatory strategies to facilitate the progress of US and Global programs and initiatives for the company. Evaluate regulations, establish framework, and design and implement science-based registration strategies for company products to ensure rapid, high-quality s

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Contract

Depends on Experience

Regulatory Affairs Specialist Small Molecule

Remote

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6d ago

Job Title: Clinical Regulatory Affairs Specialist Small Molecule Location: Remote We are seeking a Clinical Regulatory Affairs Specialist with 9+ years of experience supporting small molecule clinical development programs.Key Requirements:Strong experience in Clinical Regulatory AffairsHands-on experience with Veeva Vault TMF or similar.Experience with IND, CTA, and NDA submissionsKnowledge of ICH-Google Cloud Platform, FDA, EMA, and global regulatory requirementsExperience supporting clinical

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Contract, Third Party

Depends on Experience

Regulatory Affairs Engineer

Washington

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Today

As a Regulatory Affairs Engineer, a typical day might include the following: Maintain records of global product compliance and associated technical requirements.Track changes to regulatory requirements and determine impacts to SEL.Evaluate and research homologation requirements for markets and technologies.Sustain existing product homologation and certifications.Provide technical assistance as a content expert in worldwide product compliance.Guide engineering staff in translating product complia

Full-time

USD 97,740.00 - 144,460.00 per year

Staff Regulatory Affairs Associate (Digital Health & AI Technologies)

Boston, Massachusetts

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Today

At WHOOP, we're on a mission to unlock human performance and extend healthspan. As the leader in wearable health and performance technology, WHOOP empowers millions of members with personalized insights derived from continuous physiological monitoring, advanced analytics, and cutting-edge software experiences. WHOOP is pioneering the future of wearable health technology by combining continuous physiological monitoring, advanced analytics, and intelligent software to help millions of members imp

Full-time

USD 170,000.00 - 220,000.00 per year

Senior Spectrum Engineer, Regulatory Affairs

Remote or Carlsbad, California

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Today

About us One team. Global challenges. Infinite opportunities. At Viasat, we're on a mission to deliver connections with the capacity to change the world. For more than 35 years, Viasat has helped shape how consumers, businesses, governments and militaries around the globe communicate. We're looking for people who think big, act fearlessly, and create an inclusive environment that drives positive impact to join our team. What you'll do As a pivotal member of Viasat's global regulatory team, you

Full-time

USD 180,500.00 - 285,000.00 per year

Senior Compliance Analyst - Regulatory Exams

Dallas, Texas

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Today

Job Description The Sr. Compliance Analyst (Regulatory Exams) is responsible for supporting the network of Cetera Financial Group's broker/dealer and registered investment advisers throughout the examination process. The Regulatory Exam Manager is responsible for coordinating all aspects of firm and branch level examinations by state or federal agencies, as well as industry regulators such as FINRA. They monitor and track findings through remediation and closure and serve as the primary liaison

Full-time

USD 82,000.00 - 117,000.00 per year

Regulatory Specialist

Remote or Raynham, Massachusetts

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Today

Kelly Science and Clinical FSP is currently seeking a Regulatory Specialist for a long-term engagement with one of our Global MedTech 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 eligible

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Contract

Research Associate II - Division of Endocrinology / Department of Medicine

Los Angeles, California

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Today

Job Description Are you ready to be a part of breakthrough research? Take action now by applying to this great opportunity! Cedars-Sinai offers scientists unparalleled access to ground breaking technologies, facilities, and resources for conducting research related to an impressive range of diseases and disorders, from cancer, cardiology, and digestive diseases, to genetics, genomics, neurosciences, and women\'s health. You can continue your career journey with us! This position offers a colla

Full-time

Engineering Technician

Venice, Louisiana

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Yesterday

Summary About the Position: Serves as a senior Civil Engineering Technician with responsibility for directing the efficient andeffective accomplishment of assigned activities, providing technical guidance and instruction on workrequirements, methods and procedures; and resolving technical problems encountered bysubordinate team members. Learn more about this agency Duties Help Coordinate hydrographic reconnaissance surveys of waterways to obtain accurate data and evaluate current waterway c

Full-time

Nuclear Licensing Engineer III

Camden, New Jersey

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Today

The Nuclear Licensing Engineer is responsible for applying engineering and nuclear regulatory knowledge and experience in support of developing power plant systems and programs in accordance with US licensing requirements. This requires a demonstrated understanding of 10 CFR Parts 50 and 52, along with associated regulatory and industry guidance. The Nuclear Licensing Engineer will be part of the SMR 300 Nuclear Licensing group, which is responsible for understanding, interpreting and informing

Full-time

USD 125,000.00 per year

Computer System Validation Engineer

Wilmington, Delaware

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Today

Roles & Responsibilities : 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic reviews, access roster and audit trail reviews, Deviation/CAPA management, SOP/policy compliance processes uthoring of URS/FS, protocols, final reports, validation plan/report High-level understanding of Veeva Vault suits Risk-based testing aligned to CSA fundamentals High-level understanding of Biostatistics, Clinical, Discovery, Med

Full-time

Enterprise Systems Architect

Pearl City, Hawaii

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Today

Job ID: 2614493 Location: Pearl City, HI, US Date Posted: 2026-07-13 Category: Information Technology Subcategory: Enterprise Architect Schedule: Full-Time Shift: Day Job Travel: Yes - 10% of the time Minimum Clearance Required: Secret Clearance Level Must Be Able to Obtain: TS/SCI Potential for Remote Work: ORA_ON_SITE Description SAIC is seeking an Enterprise Systems Architect located in Pearl City, Hawaii to support the PACOM to develop, document, and analyze enterprise, operational

Full-time

USD 160,001.00 - 200,000.00 per year

Integrated Innovation for Large-Scale Problems Staff TA - College of Engineering - Integrated Innovation Institute

California

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Today

Carnegie Mellon University is a private, global research university that stands among the world's most renowned education institutions. With ground-breaking brain science, path-breaking performances, creative start-ups, big data, big ambitions, hands-on learning, and a whole lot of robots, CMU doesn't imagine the future, we invent it. If you're passionate about joining a community that challenges the curious to deliver work that matters, your journey starts here! The Integrated Innovation Insti

Part-time