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Information Technology Specialist

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Key responsabilities:

  • Lead PV Works Technical Lead
  • Manage software design and testing
  • Implement PV Works deployments
  • Serve as technical authority
  • Collaborate with team and users
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FDA Government Administration XLarge https://www.fda.gov/
10001 Employees
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Job description

This position is being filled under a stream-lined hiring authority, Title 21, Section 3072 of the 21st Century Cures Act. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority.Additional information on 21st Century Cures Act can be found here: 21st Century Cures Act InformationIntroduction The Food and Drug Administration is the regulatory, scientific, public health, and consumer protection agency responsible for ensuring that all human and animal drugs, and medical devices are safe and effective, that cosmetics, foods, food additives, drugs and medicated feeds for food producing animals, and radiation emitting devices are safe, and that all such products marketed in the United States are adequately, truthfully and informatively labeled and safely and properly stored, transported, manufactured packaged and regulated. FDA’s programs are national in scope and effect, and the agency’s activities have a direct and significant impact on multi-billion-dollar industries, in addition to protecting the health and safety of American Consumers. The work of the Agency is carried out by a staff of more than 18,000 scientists, physicians, regulatory and other personnel stationed throughout the United States. The mission of the Center for Veterinary Medicine (CVM) is to protect and promote human and animal health from a One Health perspective. CVM ensures the safety of the American food supply, the safety of animal food and devices, and the safety and effectiveness of animal drugs. Specifically, CVM evaluates new animal drug applications for safety and effectiveness and manufacturing quality; monitors animal drugs, animal foods, and animal devices for safety and takes appropriate action to mitigate unsafe or violative products on the market; evaluates animal food additives for safety and utility; conducts applied research to further scientific understanding and support data-based decision making to protect human and animal health; works to prevent and respond to human and animal health emergencies; and develops and implements policies to combat antimicrobial resistance. As a high-performance organization within the FDA, CVM strives for excellence, innovation, and leadership across all operations, occupations, and grade levels. Duties/Responsibilities - Reporting directly to the Staff Director, you will serve as the PV Works Technical Lead with responsibility for providing direction and support for the general functional and technical analysis of the software design, development, and testing lifecycle. - Manages the implementation of PV works deployments and testing in accordance to agency IT lifecycle and federal requirements. - Serves as an expert and technical authority on the development and implementation of PV Works activities and collaborating with the project management and contracting officer representative. - Trains or arranges for the training of team members in methods and techniques of team building and working in teams to accomplish tasks and complete projects. - Collaborates with business users to understand requirements and ensure solutions meet business needs.

Supervisory Responsibilities: None How to Apply Submit resume or curriculum vitae with cover letter by April 5, 2024, to: CVMOpportunities@fda.hhs.gov. Candidate resumes may be shared with hiring officials within CVM with a similar job vacancy. Candidates can opt out of this process by annotating resume with “do not share”. How I Will Be Evaluated Candidates may be evaluated based on an interview, review of requested work samples, writing samples, most recent performance evaluation(s), professional references, results of an oral presentation or work-related test. Failure to comply with any of the additional assessment requirements will result in removal from further consideration. Announcement Contact For questions regarding this Title 21 position, please contact CVMOpportunities@fda.hhs.gov. The Department of Health and Human Services is an equal opportunity employer with a smoke free environment. FDA is an equal opportunity employer.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Government Administration
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Collaboration

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