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Fda Contract Jobs in Silver Spring, MD (NOW HIRING)

NxT Level

Associate, FDA Regulations - DC

Washington, DC · On-site

$365K/yr

Draft and review regulatory submissions, compliance policies, internal procedures, and contracts * Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct ...

Westat

Principal Contracts Manager - Hybrid

Bethesda, MD · Hybrid

$95K - $127K/yr

This leadership role will provide strategic contractual guidance across the contract life cycle ... Experience supporting NIH, CDC, FDA, and/or other federal health research agencies. * Experience ...

Westat

Principal Contracts Manager - Hybrid

Bethesda, MD · On-site

$95K - $127K/yr

This leadership role will provide strategic contractual guidance across the contract life cycle ... Experience supporting NIH, CDC, FDA, and/or other federal health research agencies. * Experience ...

Stafford Consulting

CONTRACT SPECIALIST II

Tysons, VA · Remote

$50K - $65K/yr

Stafford Consulting Company, Inc. (SCC) Contract Specialist II Labor Category Contract Specialist II supporting FDA Salary Range $50,000 - $65,000 Work Location Hybrid. Remote work, but must report ...

New

Revolutional, LLC

Contracts Manager

Mclean, VA · Remote

$110K - $130K/yr

Monitor contract performance, deadlines, and deliverables; initiate renewals or amendments as ... S. Department of Agriculture (USDA), and Food and Drug Administration (FDA). * Solid understanding ...

Revolutional, LLC

Contracts Manager

Washington, DC · Remote

$110K - $130K/yr

Monitor contract performance, deadlines, and deliverables; initiate renewals or amendments as ... S. Department of Agriculture (USDA), and Food and Drug Administration (FDA). * Solid understanding ...

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Fda Contract information

See Silver Spring, MD salary details

$42.4K

$109.6K

$143.7K

How much do fda contract jobs pay per year?

As of Aug 27, 2026, the average yearly pay for fda contract in Silver Spring, MD is $109,616.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,000.00 and $123,000.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

What are the most commonly searched types of Fda jobs in Silver Spring, MD?

The most popular types of Fda jobs in Silver Spring, MD are:

What are popular job titles related to Fda Contract jobs in Silver Spring, MD?

For Fda Contract jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Fda Contract jobs in Silver Spring, MD look for?

The top searched job categories for Fda Contract jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Fda Contract jobs?

Cities near Silver Spring, MD with the most Fda Contract job openings:

Fda Contract jobs near you
Infographic showing various Fda Contract job openings in Silver Spring, MD as of August 2026, with employment types broken down into 84% Full Time, 3% Part Time, and 13% Contract. Highlights an 80% In-person, 7% Hybrid, and 13% Remote job distribution, with an average salary of $109,616 per year, or $52.7 per hour.

Associate, FDA Regulations - DC

NxT Level

Washington, DC

$225K/yr

Full-time

PTO

Re-posted 7 days ago

Job description

FDA Regulatory Associate – Health & Life Sciences Practice | Washington, DC

Our client, a nationally recognized law firm with a strong commitment to inclusivity, innovation, and well-being, is seeking an FDA Regulatory Associate with 4–5 years of experience to join its Health & Life Sciences Practice Group in Washington, DC. This is an outstanding opportunity for a motivated attorney to advise a diverse range of clients across the FDA-regulated product ecosystem, including pharmaceuticals, medical devices, biologics, health technologies, food, and cosmetics.

Key Responsibilities:

  • Advise clients on FDA regulatory matters, with a focus on drug and medical device compliance, including current good manufacturing practices (CGMP)

  • Draft and review regulatory submissions, compliance policies, internal procedures, and contracts

  • Provide legal guidance during FDA inspections, investigations, and enforcement actions

  • Conduct legal research and analysis on FDA laws, regulations, and enforcement trends

  • Collaborate with clients and internal teams to develop regulatory strategies that support business objectives

  • Stay current on evolving FDA regulations, guidance documents, and industry developments

Ideal Candidate Profile:

  • 4–5 years of experience in FDA regulatory compliance, ideally from a law firm or in-house setting

  • Demonstrated knowledge of CGMP and FDA regulatory frameworks related to drug and device development

  • Scientific background in analytical chemistry, chemical engineering, or microbiology (strongly preferred)

  • Prior experience at the Food and Drug Administration (FDA) is a plus

  • Exceptional research, analytical, and problem-solving skills

  • Outstanding written and verbal communication abilities

  • Strong academic credentials

  • Ability to thrive in a fast-paced, collaborative environment

  • Active bar membership in the District of Columbia, or eligibility to waive in through reciprocity or UBE transfer

Compensation:

This role offers a generous, merit-based compensation package, with associates regularly earning above market scale. Base salary ranges by class year:

  • 2025/2024 Class: $225,000

  • 2023 Class: $235,000

  • 2022 Class: $260,000

  • 2021 Class: $310,000

  • 2020 Class: $365,000

  • 2019 Class: $390,000

  • 2018 Class: $420,000

  • 2017 and more senior: $435,000

Why Join?

  • Award-Winning Culture: Recognized by Vault, Chambers Associate, and the Human Rights Campaign for top marks in diversity, associate satisfaction, and career development

  • Innovative Compensation Model: Associates are rewarded for performance and initiative—67% earned above the Cravath scale in 2024

  • Well-Being Focused: The firm offers billable credit for wellness, free access to the Peloton app, Lyra mental health services, and generous paid leave benefits

  • Career Development: Comprehensive coaching, mentorship, and business development support, including firm-sponsored coaching for associates achieving 250+ BD hours annually

  • Community Engagement: Up to 8 hours of billable time available for volunteer service

To Apply:

Please submit your:

  • Resume

  • Cover letter

  • Law school transcript

This is an exciting opportunity to join a market-leading FDA regulatory practice within a firm that values excellence, inclusion, innovation, and work-life balance. If you’re ready to elevate your legal career in a supportive and fast-paced environment, we encourage you to apply.

Apply