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Fda Contractor Jobs in Atlanta, GA (NOW HIRING)

MiMedx Group

Metrology Technician

Marietta, GA · On-site

$56K - $70K/yr

Coordinate and interact with equipment manufacturers, vendors, contractors and/or consultants on ... AATB, FDA, ISO and other state/federal regulations * Strong computer skills, including proficiency ...

Axelon

Material Handler

Atlanta, GA · On-site

$16 - $19.50/hr

Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ... employees, customers, contractors, and vendors. * Performs other related duties and ...

Hire Talent

Material Handler

Atlanta, GA · On-site

$20/hr

Comply with FDA regulations, company policies, operating procedures, processes, and assigned tasks. * Maintain positive communication and collaboration with employees, customers, contractors, and ...

Cynet Systems

Material Handler

Atlanta, GA · On-site

$15 - $20/hr

Compliance with U.S. Food and Drug Administration (FDA) regulations and other regulatory ... all levels of employees, contractors, and vendors. * Perform other related duties and ...

MIMEDX

Metrology Technician

Marietta, GA · On-site

$56K - $70K/yr

Coordinate and interact with equipment manufacturers, vendors, contractors and/or consultants on ... AATB, FDA, ISO and other state/federal regulations * Strong computer skills, including proficiency ...

Intellectt INC

Material Handler/inventory control

Atlanta, GA · On-site

$16 - $19.50/hr

Comply with FDA regulations, company policies, operating procedures, and standard work instructions. * Maintain positive communication and collaboration with employees, customers, contractors, and ...

Workforce Consultants

Be Seen First

Factory Facility Supervisor

White, GA · On-site

$75K/yr

Maintain high sanitation and workplace safety standards in compliance with SQF,HACCP,FDA ... Evaluate suppliers' and contractors' performances, and food safety incidents. Document all safety ...

Equiliem

Material Handler II

Atlanta, GA · On-site

$20/hr

Comply with FDA regulations, company policies, standard operating procedures, and work instructions. * Maintain positive working relationships with employees, customers, contractors, and vendors.

Equiliem

Material Handler II - Equiliem

Atlanta, GA · On-site

$20/hr

Comply with FDA regulations, company policies, standard operating procedures, and work instructions. * Maintain positive working relationships with employees, customers, contractors, and vendors.

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Showing results 1-20

All JobsFda Contractor JobsFda Contractor Jobs in Atlanta, GA

Fda Contractor information

See Atlanta, GA salary details

$28.9K

$58.5K

$85.1K

How much do fda contractor jobs pay per year?

As of Aug 4, 2026, the average yearly pay for fda contractor in Atlanta, GA is $58,497.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,600.00 and $67,300.00 per year, depending on experience, location, and employer.

What is an FDA contractor?

An FDA contractor is an individual or company that provides goods or services to the U.S. Food and Drug Administration (FDA) under a formal agreement or contract. These contractors may work in a wide range of areas including research, information technology, regulatory consulting, laboratory services, or facility maintenance. FDA contractors are not direct employees of the FDA but play a crucial role in supporting the agency’s mission to protect public health by ensuring the safety, efficacy, and security of drugs, biological products, and medical devices. Their work is often governed by strict regulations and requires compliance with federal standards. Contractors are selected through a competitive procurement process to ensure quality and value.

What are some common challenges faced by FDA contractors when working with cross-functional teams?

FDA Contractors often collaborate with diverse teams, including regulatory, quality assurance, and clinical staff. One common challenge is aligning different priorities and communication styles while ensuring compliance with regulatory standards and tight project deadlines. Success in this role requires strong organizational skills, adaptability, and proactive communication to keep projects moving smoothly and maintain regulatory integrity. Building rapport and understanding the unique needs of each department can help FDA Contractors effectively bridge gaps and facilitate teamwork.

What is the difference between Fda Contractor vs Fda Auditor?

AspectFda ContractorFda Auditor
Required CredentialsTypically requires knowledge of FDA regulations, compliance, and industry standards; certifications like RAC or CQA are commonRequires similar credentials, often with additional auditing certifications such as CQA or ISO auditor training
Work EnvironmentWorks on projects for FDA-regulated companies, often in labs, manufacturing sites, or officesConducts inspections and audits at facilities, often traveling to various sites
Employer & Industry UsageHired by pharmaceutical, biotech, or medical device companies as external consultantsEmployed by regulatory agencies or contracted to perform compliance audits for FDA oversight

In summary, Fda Contractors focus on supporting companies with compliance projects, while Fda Auditors primarily evaluate and verify adherence to FDA regulations through inspections and audits. Both roles require similar certifications and industry knowledge but differ in their primary functions and work settings.

What are the key skills and qualifications needed to thrive as an FDA contractor?

To thrive as an FDA Contractor, you need expertise in regulatory compliance, scientific analysis, and project management, often supported by a degree in life sciences or a related field. Familiarity with FDA regulations, electronic submission systems, and specialized software like eCTD or data analysis tools is typically required. Attention to detail, strong communication skills, and adaptability help contractors excel in collaborative and deadline-driven environments. These skills ensure accurate, timely submissions and effective support for FDA regulatory processes.
What are popular job titles related to Fda Contractor jobs in Atlanta, GA? For Fda Contractor jobs in Atlanta, GA, the most frequently searched job titles are:
What job categories do people searching Fda Contractor jobs in Atlanta, GA look for? The top searched job categories for Fda Contractor jobs in Atlanta, GA are:
What cities near Atlanta, GA are hiring for Fda Contractor jobs? Cities near Atlanta, GA with the most Fda Contractor job openings:
Fda Contractor jobs near you
Infographic showing various Fda Contractor job openings in Atlanta, GA as of July 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 82% In-person, and 18% Remote job distribution, with an average salary of $58,497 per year, or $28.1 per hour.

Remote Regulatory Affairs contractor

Globalchannelmanagement

Atlanta, GA • Remote

$99 - $100/hr

Full-time

Re-posted 8 days ago

Job description

Remote Regulatory Affairs contractor requires:

  • Bachelor's degree in engineering, life sciences, regulatory affairs, legal or a related field
  • 5-10 years+ of global medical device regulatory experience
  • Proven experience preparing, writing and submitting FDA 510k submissions (end to end)
  • Experience with ophthalmic devices, capital equipment, diagnostic devices, software in medical devices, cybersecurity
  • Strong working knowledge of:
    • FDA regulations (21 Parts 807, 820)
    • FDA guidance documents and eStar requirements
    • Experience with Canadian regulations, EU MDR (2017/745) including Class lla, Tech docs Annex ll/lll
  • Demonstrated ability to work independently as a contractor in a fast-paced environment
  • Experience filing medical device submissions in China and other countries
  • Experience with audiology devices
  • Experience with artificial-intelligence enabled devices
  • Strong technical writing and documentation skills
  • Ability to translate complex technical information into regulatory submissions
  • Detail-oriented with strong organization skills
  • Effective communicator across technical and non-technical stakeholders
  • Ability to manage multiple deliverables and timelines

DUTIES:

  • FDA 510(k) submission
  • Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliance
  • Perform detailed regulatory gap assessments against FDA requirements (21 CFR Parts 807, 820, and applicable FDA guidance documents)
  • Author, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format,
  • Lead submission lifecycle activities, including:
    • Acceptance Review support (RTA readiness)
    • Substantive Review coordination
    • Drafting and submission of responses to FDA requests for Additional Information, Interactive review communications
    • Updating submission content and modules as required
  • Interface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process.
  • Provide regulatory leadership through FDA clearance.
  • EU MDR Technical Documentation Support
  • Conduct EU MDR readiness assessment aligned with Notified Body expectations and conformity assessment requirements.
  • Perform critical review and gap analysis of EU MDR technical file
  • Provide targeted recommendations to ensure audit-readiness and Notified Body acceptance
  • Lead or support submission to obtain CE Mark
  • Health Canada submission
  • Global Regulatory Strategy and Advisory