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

Tunnell Government Services

Ophthalmology SME

Bethesda, MD · On-site

$20 - $27/hr

FDA CDRH - Ophthalmology SME Position Description The mission of the FDA Center for Devices and ... Tunnell employees and/or contractors are expected to comply with all client requirements, including ...

Tunnell Government Services

Ophthalmology SME

Bethesda, MD · On-site

$20 - $27/hr

FDA CDRH - Ophthalmology SME Position Description The mission of the FDA Center for Devices and ... Tunnell employees and/or contractors are expected to comply with all client requirements, including ...

Tunnell Government Services

Urology SME

Bethesda, MD · On-site

FDA CDRH - Urology SME Position Description The mission of the FDA Center for Devices and ... Tunnell employees and/or contractors are expected to comply with all client requirements, including ...

Tunnell Government Services

Ophthalmology SME

Washington, DC

$21.25 - $28.50/hr

FDA CDRH - Ophthalmology SME Position Description The mission of the FDA Center for Devices and ... Tunnell employees and/or contractors are expected to comply with all client requirements, including ...

Tunnell Government Services

Urology SME

Bethesda, MD · On-site

FDA CDRH - Urology SME Position Description The mission of the FDA Center for Devices and ... Tunnell employees and/or contractors are expected to comply with all client requirements, including ...

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Showing results 1-20

All JobsFda Contractor JobsFda Contractor Jobs in Silver Spring, MD

Fda Contractor information

See Silver Spring, MD salary details

$31K

$62.9K

$91.5K

How much do fda contractor jobs pay per year?

As of Jul 1, 2026, the average yearly pay for fda contractor in Silver Spring, MD is $62,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,100.00 and $72,400.00 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, and why are they important?

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 job categories do people searching Fda Contractor jobs in Silver Spring, MD look for? The top searched job categories for Fda Contractor jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Fda Contractor jobs? Cities near Silver Spring, MD with the most Fda Contractor job openings:
Fda Contractor jobs near you
Infographic showing various Fda Contractor job openings in Silver Spring, MD as of June 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 82% In-person, 3% Hybrid, and 15% Remote job distribution, with an average salary of $62,884 per year, or $30.2 per hour.

EHS Manager (GMP experience required)

Granules

Chantilly, VA • On-site

$95K - $115K/yr

Full-time

Posted 15 days ago

Job description

Description:

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.


We are seeking a highly experienced EHS Manager to lead and oversee Environmental, Health, and Safety (EHS) programs across our pharmaceutical operations in Chantilly and Manassas, Virginia. This role is responsible for ensuring full regulatory compliance, minimizing risk, and driving a strong safety culture across both sites.


Key Responsibilities


  • Manage and oversee all EHS programs for the Chantilly and Manassas manufacturing sites
  • Develop, implement, and continuously improve safety policies, procedures, and site-specific safety plans.
  • Ensure compliance with OSHA, FDA, EPA, GMP, and applicable state and local regulations
  • Lead site risk assessments, job hazard analyses, and safety audits
  • Investigate incidents, near-misses, and safety concerns; implement corrective and preventive actions (CAPA)
  • Oversee chemical safety, hazardous material handling, waste management, and emergency response programs
  • Plan and deliver safety training for employees, contractors, and visitors
  • Track, analyze, and report safety performance metrics; recommend improvement initiatives
  • Serve as the primary contact for regulatory inspections, audits, and external agencies
  • Partner with operations, quality, and engineering teams to integrate safety into daily activities and project.
  • Support GMP environments by ensuring safe manufacturing practices without compromising product quality


Requirements:


Required Qualifications


  • Bachelor’s degree in occupational health & safety, Environmental Science, Engineering, or related field.
  • Minimum 5–7 years of EHS or safety management experience in a pharmaceutical, biotech, or regulated manufacturing environment.
  • Strong working knowledge of OSHA, FDA, GMP, EPA, and industrial safety regulations.
  • Experience managing multi-site operations preferred.
  • Professional certifications such as CSP, ASP, NEBOSH, or equivalent strongly preferred.
  • Excellent leadership, communication, and organizational skills.
  • Ability to travel regularly between Chantilly and Manassas sites.


What We Offer


  • Competitive salary and comprehensive benefits package.
  • Opportunity to lead safety programs across multiple pharmaceutical sites.
  • Collaborative, quality-driven work environment.
  • Career growth and long-term stability.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.