1

Fda Jobs in Virginia (NOW HIRING)

This role is responsible for operating manufacturing equipment, executing batch processes, maintaining compliance with SOPs and FDA regulations, and ensuring safe, efficient, and high-quality ...

This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines. * The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP ...

Cloud Architect

Sterling, VA ยท On-site

$140 - $190/hr

Lead the design and implementation of secure, scalable, resilient, and cost-effective cloud architectures supporting enterprise FDA applications. * Define target-state cloud architectures ...

Cloud Architect

Sterling, VA ยท On-site

$64.25 - $82/hr

... FDA applications and services. The Cloud Architect will provide technical leadership across cloud architecture, application modernization, DevSecOps, security, infrastructure automation, cloud-native ...

Showing results 21-40

Fda information

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in Virginia?

The most popular types of Fda jobs in Virginia are:

What cities in Virginia are hiring for Fda jobs?

Cities in Virginia with the most Fda job openings:

Infographic showing various Fda job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Production Operator II

Mintex Technology

Chantilly, VA โ€ข On-site

$76K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 19 days ago


Job description

Title : Production Operator II / III – Pharmaceutical Manufacturing
Location: Chantilly, VA
Job Type: Full-Time
Salary: $76000/yr plus $3000 joining bonus
Industry: Pharmaceutical Manufacturing
Benefits:
  • Competitive compensation
  • Health, Dental & Vision Insurance
  • 401(k) & Company Benefits
  • Training & Career Growth Opportunities
  • Stable pharmaceutical manufacturing environment
Position Overview:
We are seeking experienced Production Operators II & III with strong OSD (Oral Solid Dosage) manufacturing experience to support pharmaceutical production operations in a cGMP-regulated environment. This role is responsible for operating manufacturing equipment, executing batch processes, maintaining compliance with SOPs and FDA regulations, and ensuring safe, efficient, and high-quality production.
Candidates should have hands-on experience in one or more areas including Compression, Encapsulation, Coating, Granulation, Blending, or Wurster Coating.
Key Responsibilities:
  • Operate pharmaceutical manufacturing equipment for weighing, blending, granulation, compression, encapsulation, coating, drying, milling, and dispensing
  • Perform equipment setup, cleaning, batch changeovers, and line clearance activities per SOPs
  • Execute batch production processes and complete Batch Production Records (BPRs) accurately
  • Conduct in-process quality checks, sampling, and documentation in compliance with cGMP and FDA standards
  • Troubleshoot production and equipment issues to minimize downtime
  • Maintain cleanroom, safety, and PPE compliance standards
  • Support continuous improvement, Lean Manufacturing, and process optimization initiatives
  • Collaborate with production, quality, and maintenance teams to meet production schedules and quality goals
Required Qualifications:
  • High School Diploma or GED required
  • 2–5+ years of pharmaceutical manufacturing experience in OSD production
  • Strong knowledge of cGMP, FDA regulations, and SOP compliance
  • Experience with Compression, Encapsulation, Coating, Granulation, or Blending operations
  • Hands-on experience with pharmaceutical equipment such as Fette tablet presses, MG2 encapsulation machines, Korsch XM 12, or similar
  • Experience with Glatt, Pan Coating, or Wurster Coating preferred
  • Ability to perform equipment cleaning, setup, and troubleshooting
  • Strong documentation, communication, and teamwork skills
  • Ability to work 12-hour shifts, lift up to 50 lbs, and wear required PPE
Preferred Skills:
  • Lean Manufacturing & Six Sigma knowledge
  • Batch record documentation and QA/QC procedures
  • Forklift certification (preferred)
  • Strong mechanical aptitude and problem-solving skills