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Fda Openings Jobs in Reston, VA (NOW HIRING)

... FDA IT systems o Provide excellent customer service o Communicate effectively with peers and ... opening mail, calculating and posting charges to departmental accounts, operating basic office ...

... FDA IT systems o Provide excellent customer service o Communicate effectively with peers and ... opening mail, calculating and posting charges to departmental accounts, operating basic office ...

... FDA IT systems o Provide excellent customer service o Communicate effectively with peers and ... opening mail, calculating and posting charges to departmental accounts, operating basic office ...

Provide technical support for radiation safety and health physics programs at FDA facilities ... To view all of our open positions, and to apply to those positions in which you may be interested ...

This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines. * The ... Lead the communication of open quality document notification and resolution between all departments ...

Provide technical support for radiation safety and health physics programs at FDA facilities ... To view all of our open positions, and to apply to those positions in which you may be interested ...

Java Developer

Rockville, MD · On-site

$52 - $67.25/hr

Salient CRGT will not sponsor applicants for work visas for this opening. DESIRED EXPERIENCE: * Previous experience working with the US Food and Drug Administration (FDA) is a plus. Experience with ...

Java Developer

Rockville, MD · On-site

$52 - $67.25/hr

Salient CRGT will not sponsor applicants for work visas for this opening. DESIRED EXPERIENCE: * Previous experience working with the US Food and Drug Administration (FDA) is a plus. Experience with ...

Provide technical guidance and support for radiation safety and health physics programs at FDA ... To view all of our open positions, and to apply to those positions in which you may be interested ...

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Fda Openings information

What are the key skills and qualifications needed to thrive in FDA job openings, and why are they important?

To thrive in FDA job openings, candidates typically need a strong background in science, regulatory affairs, and analytical skills, often with a relevant degree in biology, chemistry, pharmacy, or related fields. Familiarity with regulatory databases, submission systems (such as eCTD), and certifications like RAC (Regulatory Affairs Certification) are highly valued. Attention to detail, effective communication, and the ability to work collaboratively are essential soft skills for success. These competencies ensure regulatory compliance, thorough review of submissions, and effective teamwork in safeguarding public health.

What are some common challenges faced by professionals starting in FDA roles, and how can applicants prepare for them?

Professionals beginning their careers at the FDA often encounter challenges such as adapting to complex regulatory frameworks, working with cross-disciplinary teams, and managing the pace of policy changes. To prepare, applicants should familiarize themselves with FDA guidelines and regulatory processes, develop strong communication skills to collaborate effectively with scientists, regulators, and industry representatives, and stay updated on current public health issues. Proactive learning and seeking mentorship within the organization can also ease the transition and foster professional growth.

What are FDA openings?

FDA openings refer to job opportunities or vacancies at the U.S. Food and Drug Administration (FDA). The FDA is a federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other related products. These openings span a wide range of roles, including scientists, inspectors, analysts, administrative professionals, and more. Candidates can find current job listings and application instructions on the official USAJOBS website and the FDA’s careers page. Working at the FDA offers the chance to contribute to public health and safety at a national level.

Records Management Specialist I (General Clerk)

MPF Federal

College Park, MD • On-site

$18/hr

Full-time

Medical, PTO

Posted 26 days ago


Job description

MPF Federal is bringing on a Records Management Specialist 1 (general clerk) to support the FDA's regulatory mission by keeping critical documents organized, accurate, and moving. You'll work onsite with FDA division personnel, handling the documents that keep regulatory reviews on track. This is steady, detail-driven work with clear processes, direct supervision, and room to build federal contracting experience.

COMPENSATION: $18.00 per hour

*This is a hybrid position with onsite work in College Park, MD*

What You'll Do
  • Process, classify, and label FDA regulatory documents using multiple data entry systems
  • Perform data entry, scanning, filing, indexing, and file maintenance for physical and electronic records
  • Prepare acknowledgement letters, memorandums, forms, and standard reports
  • Open, process, and distribute incoming mail; create and affix barcode labels
  • Retrieve documents and information in response to user requests
  • Provide clerical and administrative support to project staff

Requirements

  • High school diploma or equivalent plus 1 to 2 years of related administrative or data entry experience
  • Strong computer skills and the ability to perform data entry
  • Good organizational and interpersonal skills and a team-first attitude
  • Ability to lift and move standard boxes up to 30 lbs
  • Willingness to learn regulatory terminology and become the go-to person for your unit's files

Benefits

MPF Federal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. We offer a competitive compensation package including a competitive salary, medical benefits, PTO, holiday pay and more.