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Fda Contract Jobs (NOW HIRING)

Birdi Systems, Inc.

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Program Manager - Security Systems

Silver Spring, MD · On-site

$130K - $150K/yr

Birdi Systems, Inc. is seeking an experienced Program Manager to provide commercial and technical leadership for a $40M FDA contract supporting security systems maintenance and move, add, and change ...

NxT Level

Associate, FDA Regulations - DC

Washington, DC · On-site

$225K/yr

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

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Fda Contract information

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$106K

$139K

How much do fda contract jobs pay per year?

As of Jun 22, 2026, the average yearly pay for fda contract in the United States is $106,034.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $119,000.00 per year, depending on experience, location, and employer.

What is an FDA Contract job?

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.

More about Fda Contract jobs
What cities are hiring for Fda Contract jobs? Cities with the most Fda Contract job openings:
What are the most commonly searched types of Fda jobs? The most popular types of Fda jobs are:
What states have the most Fda Contract jobs? States with the most job openings for Fda Contract jobs include:
What job categories do people searching Fda Contract jobs look for? The top searched job categories for Fda Contract jobs are:
Fda Contract jobs near you
Infographic showing various Fda Contract job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 40% Full Time, 11% Part Time, and 46% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $106,034 per year, or $51 per hour.
Technical Writer - FDA

Technical Writer - FDA

DRT Strategies

Silver Spring, MD • On-site

Full-time

Posted 6 days ago

Job description

Job Summary:
DRT Strategies is a consulting firm that provides management consulting and IT solutions to federal agencies and commercial clients. They are seeking a Technical Writer to support the FDA's Center for Drug Evaluation and Research by drafting, reviewing, and editing compliance-related documentation while ensuring adherence to federal requirements and FDA guidelines.
Responsibilities:
• Draft, review, and edit warning letters issued to regulated entities for violations of FDA regulations, ensuring technical accuracy, regulatory citation precision, and adherence to FDA's warning letter format, tone, and enforcement policies.
• Develop and edit import alert documentation for products subject to detention without physical examination, ensuring clarity in describing violations, affected products, and guidance for industry compliance, while maintaining consistency with Customs and Border Protection coordination requirements.
• Draft policy statements and guidance documents outlining FDA's enforcement discretion positions, ensuring clear articulation of scope, conditions, and limitations, and verifying alignment with applicable statutory and regulatory frameworks.
• Prepare briefing documents, meeting agendas, summary reports, and presentation materials for regulatory meetings with industry, advisory committees, and other stakeholders; edit meeting minutes and follow-up correspondence for accuracy and completeness.
• Analyze and synthesize performance data related to FDA's annual reporting requirements and draft narrative sections explaining performance outcomes, trends, and contextual factors.
• Develop concise, accurate talking points for FDA leadership and staff communications with external stakeholders, adapting technical content for diverse audiences including industry, consumer advocates, Congress, and media.
Qualifications:
Required:
• A minimum of 5–8 years of professional experience in technical writing, preferably within federal contracts or the Department of Defense (DoD) environment.
• Demonstrated expertise in federal regulatory writing and FDA-specific documentation standards is strongly preferred.
• Proven ability to incorporate feedback from subject matter experts and legal reviewers efficiently and meet established deadlines while maintaining high quality standards.
• Experience handling sensitive or pre-decisional government information with strict confidentiality.
• Familiarity with a style guide (e.g., AP, AMA).
• A Bachelor's degree in one of the following fields: English, Journalism, Communications, Engineering, or a technical discipline (Engineering, Computer Science, Biological sciences).
• This position requires the ability to obtain and maintain a U.S. government Public Trust clearance.
• Due to contract requirements, candidates must be U.S. citizens or lawful permanent residents (green card holders) to be eligible.
Preferred:
• Experience with the FDA, regulatory, healthcare, laboratory, pharmaceutical industry.
• Advanced proficiency in MS Office Suite (Word, Excel, PowerPoint, etc.) and tools such as SharePoint and Adobe Acrobat.
• Experience with Visual Basic, EndNote, Adobe Acrobat.
• Familiarity with Section 508 compliance.
Company:
DRT Strategies is a management consulting company that offers information technology, project management, and financial management services. Founded in 2004, the company is headquartered in Arlington, USA, with a team of 201-500 employees. The company is currently Growth Stage.

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