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Fda Gov Jobs (NOW HIRING)

Vitalief

Clinical Research Coordinator

Philadelphia, PA · On-site

$24.50 - $32.50/hr

... FDA, IRB, and GCP guidelines. * Monitor safety events, prepare reports, and support sponsor/audit visits. * Maintain study records (OnCore, Epic, ClinicalTrials.gov) and oversee research billing ...

Vitalief

Clinical Research Coordinator

Philadelphia, PA · On-site

$23.25 - $30.75/hr

... FDA, IRB, and GCP guidelines. * Monitor safety events, prepare reports, and support sponsor/audit visits. * Maintain study records (OnCore, Epic, ClinicalTrials.gov) and oversee research billing ...

State of Virginia

Relief Pharmacist

Roanoke, VA

$69.50/hr

Davis & McDaniel Vet Care Ctr Agency Website: www.dvs.virginia.gov Recruitment Type: General Public ... Is knowledgeable of and follows laws and regulations pertaining to pharmacy as set forth by FDA ...

B&G Foods

FSQA Manager

Cincinnati, OH

Experience with FDA Acidified Foods standards * Experience in Microbiological and Analytical ... gov/employers/upload/eeoc_self_print_poster.pdf.

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How much do fda gov jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for fda gov in the United States is $12.66, according to ZipRecruiter salary data. Most workers in this role earn between $10.82 and $13.46 per hour, depending on experience, location, and employer.

What types of cross-functional teams do FDA government employees typically work with, and how does this collaboration impact daily responsibilities?

FDA government employees frequently collaborate with interdisciplinary teams that may include scientists, legal experts, policy analysts, and public health professionals. This cross-functional teamwork ensures that regulatory decisions are well-rounded and scientifically sound. On a daily basis, employees may participate in meetings to review data, discuss policy implications, or coordinate responses to public health concerns. The collaborative environment fosters comprehensive problem-solving and helps employees gain a broader understanding of the regulatory landscape.

What is the difference between Fda Gov vs Food Safety Specialist?

AspectFda GovFood Safety Specialist
CertificationsVaries; often includes regulatory or compliance trainingOften requires food safety certifications like ServSafe or HACCP
Work EnvironmentGovernment agencies, offices, laboratoriesFood production facilities, inspection sites, laboratories
Employer & IndustryU.S. Food and Drug Administration, government sectorFood manufacturing, retail, consulting

Fda Gov typically refers to roles within the FDA or related government agencies focusing on regulation and compliance. Food Safety Specialists work in the food industry, ensuring safety standards are met. While both roles involve food safety, Fda Gov positions are more regulatory and policy-oriented, whereas Food Safety Specialists focus on practical implementation and inspection in the industry.

What does the FDA do?

The U.S. Food and Drug Administration (FDA) is a federal agency responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices. The FDA also oversees the safety of the nation’s food supply, cosmetics, and products that emit radiation. In addition, the FDA regulates tobacco products and works to advance public health by helping speed innovations that make medical products safer and more effective.

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 typically need a background in life sciences or related fields, along with knowledge of regulatory guidelines and compliance standards. Familiarity with submission management systems, regulatory databases, and certifications such as RAC (Regulatory Affairs Certification) are highly valuable. Strong attention to detail, analytical thinking, and effective communication skills help professionals excel when interpreting complex regulations and working with cross-functional teams. These capabilities ensure accurate, timely submissions and help organizations maintain compliance with FDA regulations, which is critical for product approvals and market access.
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What cities are hiring for Fda Gov jobs? Cities with the most Fda Gov job openings:
What states have the most Fda Gov jobs? States with the most job openings for Fda Gov jobs include:
What job categories do people searching Fda Gov jobs look for? The top searched job categories for Fda Gov jobs are:
Fda Gov jobs near you
Infographic showing various Fda Gov job openings in the United States as of May 2026, with employment types broken down into 79% Full Time, 18% Part Time, 1% Temporary, and 2% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $26,341 per year, or $12.7 per hour.

Instructional Designer

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

$60K - $81K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Job description

Job Description Header:
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for an Instructional Designer in Boca Raton, FL!
Job Title: Instructional Designer
Job Description:
Position Summary
The Instructional Designer, a member of our Training & Development team, will be responsible for designing, developing, and implementing engaging and effective training programs tailored to our scientific, technical, and compliance-driven environment. The Instructional Designer will collaborate with subject matter experts (SMEs), trainers/training coordinators, and leadership to create learning solutions that support employees in plasma collection and manufacturing operations.
Essential Functions (ES) and Responsibilities
  • Instructional Design & Development: Create high-quality and engaging learning materials, including eLearning modules, instructor-led training (ILT), virtual instructor-led training (vILT), microlearning, job aids, and assessments tailored to adult learners.
  • Needs Analysis: Conduct training needs assessments to identify learning gaps and propose effective instructional strategies.
  • Collaboration: Work closely with SMEs, scientists, compliance officers, and cross-functional teams to develop accurate and engaging content.
  • Technology & Tools: Utilize authoring tools (Grok, VistaCreate, Camtasia, etc.), electronic quality management systems (eQMS), and other eLearning platforms to design and deploy training solutions.
  • Compliance & Regulatory Training: Ensure that all learning programs meet industry-specific regulatory and compliance standards (e.g., FDA, GMP, GCP, GLP, GxP, CLIA).
  • Evaluation & Improvement: Implement feedback mechanisms, track learning effectiveness using data analytics, and continuously improve training content.
  • Project Management: Manage multiple instructional design projects, ensuring timely delivery and alignment with business objectives.

Education and Experience Requirements
Education Requirements: Minimum of a Bachelor's degree in Instructional Design, Education, Life Sciences or a related field with a training and development focus.
Experience Requirements:
  • Three plus years of instructional design experience, preferably in the biopharmaceutical, pharmaceutical, biotechnology, or healthcare industry.
  • Experience working in regulated environments with a focus on Compliance training.
  • Strong knowledge of adult learning theories, instructional design models and training methodologies.
  • Strong project management and organizational skills.
  • Ability to communicate complex scientific and technical information in an engaging, learner-friendly manner.
  • Excellent collaboration skills.
  • Technical Skills.
  • Proficiency in eLearning development tools (e.g., Audiate, Camtasia, WellSaid, Vista Create, PearDeck, Kahoot, Grok).
  • Experience with LMS/eQMS administration and SCORM/xAPI standards.
  • Familiarity with multimedia design, video editing, and graphic design tools (e.g., Camtasia, Canva, Vyond, Photoshop) is a plus.

Compliance Requirements (ES)
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
Job Description Footer:
In addition to competitive compensation, we offer a comprehensive benefits package including:
  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance
  • Company paid STD and LTD
  • Company Paid Holidays
  • 3 Weeks' Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)
  • Easily accessible to Tri-Rail. Free shuttle to the Boca Tri-Rail station

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
ADMA Biologics is an Equal Opportunity Employer.

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