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Fda Contract Jobs (NOW HIRING)

Astrix Inc

QA Auditor (FDA/GMP/21 CFR)

Lancaster, SC · On-site

... CMOs, and contract laboratories. This is a highly visible position within QA, responsible for ensuring compliance with FDA regulations and strengthening supplier quality programs. Key ...

Prenosis, Inc.

Contract Administrator

Chicago, IL · On-site +1

$28.85 - $38.46/hr

We've created and validated the first FDA-authorized AI biomarker for sepsis, the Sepsis ... The Contract Administrator is responsible for managing, preparing, reviewing, and analyzing ...

VB Spine

Contracts & Proposal Senior Analyst

Leesburg, VA · On-site

$100K/yr

... g., FDA, Sunshine Act). * Support audits and internal reporting related to contract performance, compliance, and customer pricing history. * Ensure all documentation aligns with current regulatory ...

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$41K

$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.

Surgical Oncologist - FDA

Tunnell Government Services

Bethesda, MD • On-site

Full-time

Posted 11 days ago

Job description

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
FDA CDRH - Medical Officer (Surgical Oncologist) SME Position Description
The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.
Tunnell Government Services, Inc. is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices.In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH's projects.
Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in surgical oncology, as relevant to medical devices.
Requirements and Qualifications
  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • In addition, the candidate must possess a current, active, full, and unrestricted medical license or registration as a Physician to practice medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • At least ten (10) years of relevant clinical experience
  • Certification from a U.S. relevant specialty board organization, e.g., the American Board of Surgery (ABS), Society of Surgical Oncology (SSO), etc.
  • Thorough understanding of current clinical practices in surgical oncology, including diagnosis and treatment, and current/emerging trends in practice.
  • Expert in function and utilization of medical devices commonly used as part of surgical oncology (e.g., advanced energy and resection devices [electrosurgical units, ultrasonic scalpels, argon beam coagulators], minimally invasive and robotic platforms [robotic-assisted surgery systems, laparoscopes and thoracoscopes], localization and navigation devices [tumor localization seeds, intraoperative ultrasound], tumor ablation systems [radiofrequency ablation and microwave ablation, cryoablation systems, irreversible electroporation], lymph node mapping systems [gamma probes, near-infrared fluorescence imaging], intraoperative therapy devices [hyperthermic intraperitoneal chemotherapy pumps, intraoperative radiation therapy systems]).
  • Familiarity with relevant FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 878 - General and Plastic Surgery Devices), and guidances is preferred.
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.

This position is 100% telework.
Must be a US Citizen or a Full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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