Skip to Job Postings

62,518 FDA Regulatory Jobs

Within 5000 miles of Ashburn, VA
General Dynamics Information Technology

Regulatory Affairs Specialist - FDA

General Dynamics Information Technology Fort Deterick, MD
  • Type
    Full-Time

The Regulatory Affairs Scientist will ensure compliance with FDA Sponsor responsibilities, serve as a subject matter expert for regulatory strategy, to include identifying and mitigating risk, and ...

Sterling Life Sciences

Director of Regulatory Science and Policy

Sterling Life Sciences Washington, DC
  • Type
    Full-Time

... FDA on initiatives, such as the company FDA regulatory science and policy fellowship and oversee a wide array of relevant tasks and assignments that will advance the company's mission 9) Develop and ...

Organon & Co.

Director, Regulatory Legal

Organon & Co. Alexandria, VA
  • Type
    Full-Time

Advising the organization on FDA regulatory issues and compliance with laws, regulations, and applicable standards and policies throughout a drug or device's lifecycle, including research, regulatory ...

  • Type
    Full-Time

US FDA). Under the direction of the Director or Senior Director, Regulatory Affairs, this individual will support various regulatory application types including INDs, NDAs, BLAs, and related ...

ICON

Sleep Laboratory Manager

ICON Silver Spring, MD
  • Type
    Full-Time

Teach practices (FDA regulations, rules, and policies affecting conduct, record-keeping, and monitoring of human protocols involving investigational new drugs.) to others (students, enlisted soldiers ...

FEFA LLC

Medical Writer

FEFA LLC Fort Belvoir, VA
  • Type
    Contractor

Interpret information into clear and concise scientific writing and apply applicable FDA regulations for the writing and publishing of regulatory submissions. * Write, review, and edit multi-volume ...

Kikiktagruk Inupiat Corporation

Sleep Laboratory Manager

Kikiktagruk Inupiat Corporation Silver Spring, MD
  • Type
    Full-Time

Knowledge of/experience with FDA regulations, rules, and policies affecting conduct, record-keeping, and monitoring of human protocols involving investigational new drugs. * Ability to teach these ...

Actalent

Serology Medical Technologist I

Actalent Silver Spring, MD
  • Type
    Full-Time

SOPs, manufacturer guidelines and CAP/ FDA regulations. Ensures proper handling of samples, data entry, aliquoting of samples for storage, retrieval of samples, and the monitoring of laboratory ...

Medela AG

Manager of Regulatory Affairs

Medela AG McHenry, IL
  • Type
    Full-Time

Subject matter expert in FDA regulations, standards, documentation, and labeling * Strong knowledge in 13485, 14971, MDD, FDA cGMP's, FDA QSR's, UL, CE, IEC Standard, 21 CFR, etc. Medela's US-based ...

Logistics Management Institute

Project Analyst

Logistics Management Institute Frederick, MD

Experience with medical product development, DoD test and evaluation, and regulatory approval processes desired * Knowledge of DOD 5000.02, Federal Acquisition Regulations, and FDA regulations

Otsuka Pharmaceutical Co., Ltd.

Senior Director, Corporate Counsel

Otsuka Pharmaceutical Co., Ltd. Rockville, MD
  • Type
    Full-Time

Maintain a deep and current awareness of evolving FDA and OPDP regulations and interpretations, advisory comments, enforcement actions and policy issues; * Oversee Legal Affairs promotional review ...

Kikiktagruk Inupiat Corporation

Sleep Laboratory Research Manager

Kikiktagruk Inupiat Corporation Bethesda, MD
  • Type
    Full-Time

Knowledge of/experience with FDA regulations, rules, and policies affecting conduct. * Ability to teach practices to students and other staff. * Knowledge of all current guidelines for ...

Fresenius Kabi

SENIOR FDA COMPLIANCE MANAGER

Fresenius Kabi Washington, DC
  • Type
    Full-Time

Compliance evaluations of investigations and changes that could have an impact on regulatory commitments. * Responsible for preparation of manufacturing sites and I&D centers for US-FDA inspections ...

MERIT MEDICAL SYSTEMS

Senior Regulatory Affairs Specialist

MERIT MEDICAL SYSTEMS South Jordan, UT
  • Type
    Full-Time

Prepares regulatory submissions to the FDA, the Notified Body and other regulatory authorities. * Prepares IDEs and PMAs and assists with clinical trials when required. * Interacts with various ...

CAMRIS

Medical Writer

CAMRIS Frederick, MD
  • Type
    Full-Time

Understanding of FDA regulatory documentation requirements. Preferred * RAC (US) is preferred but not required. * EDMS experience. * Experience writing, reviewing, and/or editing Common Technical ...

MERIT MEDICAL SYSTEMS

Principal Regulatory Affairs Specialist

MERIT MEDICAL SYSTEMS South Jordan, UT
  • Type
    Full-Time

Interact directly with the FDA and/or indirectly with international regulatory agencies on most products/projects at reviewer level; all significant issues will be reviewed with management

FUJIFILM

Sr Regulatory Affairs Manager

FUJIFILM California City, CA

FUJIFILM Irvine Scientific adheres to both ISO and FDA regulations and operates dual cGMP manufacturing facilities in California, USA, and Tokyo, Japan. The company's consultative philosophy combined ...