Investigator II

We need to output HTML fragment with sections: Duties Summary? Actually the posting includes "Duties Summary" then "Requirements Qualifications". There's no explicit "Responsibilities" etc. We need to use

for section headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We should map content to appropriate headings. We have Duties Summary: that could be "Responsibilities". Also there is description of duties. So we can put

Responsibilities

with paragraphs and maybe list. We have Requirements Qualifications: that could be "Requirements" or "Qualifications". We'll have both maybe. The content includes basic qualification requirements, education/experience requirement. So we can put

Requirements

and maybe

Qualifications

but we should avoid thin sections. Could combine into one "Requirements" section containing both. We also have location info etc. Could be "About the role" maybe. But we have no explicit "About the role". Could put location and agency description under "About the role". The posting includes description of FDA, HHS, etc. That could be "About the role". We'll include that. We must not include boilerplate like EEO etc. There's none. We must not include Pay/Benefits/Schedule unless stated. Not present. We must not repeat job title as heading. We must not include Job ID etc. We need to preserve all substantive info. We need to use

• for any list of duties/requirements/benefits. So we need to identify lists. In Duties Summary: there are sentences describing duties; we could turn them into a list? The instruction: use
  • for any list of duties/requirements/benefits. If the content is not already a list, we could still format as paragraphs? It says use
    • for any list of duties/requirements/benefits. If it's not a list, we can use

      . So we can keep paragraphs. In Requirements: there is a list of education/experience options (bulleted with -OR-). That's a list; we should convert to

      • . Also there is list of scientific fields; that's also a list. Also list of comparable experience definition maybe. We need to preserve all info. Let's extract sections: About the role: description of position, mission, agency, location. Responsibilities: duties summary paragraphs. Requirements: basic qualification requirements description, education/experience requirement (with options), note about transcripts, etc. Qualifications: maybe we can combine with Requirements; but we could have a separate "Qualifications" section for the list of scientific fields etc. However the instruction: prefer a few substantive sections over many thin ones. So maybe combine Requirements and Qualifications into one "Requirements" section. But we have headings list: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We can choose to include About the role, Responsibilities, Requirements. That's three sections. We must not create empty sections. Now craft HTML. We need to preserve all substantive info: include the legal citation, pay table, etc. That's in Duties Summary? Actually first paragraph: "This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 1, Band A (GS-11 equivalent)." This is substantive; we should include it maybe under About the role or Responsibilities? It's about appointment type and pay table. Could be part of About the role. We'll put that in About the role paragraph. Now Responsibilities: The duties summary paragraph after that: "The candidate selected for this position will serve under a career or career-conditional appointment...". Actually that's already used. The duties summary includes: "The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority." That's more about appointment. Then later: "This position is being recruited based on the Title 21 Pay Table 1, Band A (GS-11 equivalent)." That's also about pay. But the duties summary also includes: "The position investigates and/or inspects FDA-regulated industry globally and evaluates compliance..." etc. That's the core duties. We'll separate: maybe first paragraph about appointment/pay goes to About the role. Then the rest of duties summary goes to Responsibilities. Let's parse the text: "Duties Summary This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 1, Band A (GS-11 equivalent). The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 1, Band A (GS-11 equivalent)." Actually appears duplicated? The text repeats. We'll keep once. Then after that: "Requirements Qualifications In order to qualify for the Investigator II position which falls under the 0696 occupational Series, you must meet the following requirements by 11:59 pm EST on 10/01/2026: Basic Qualification Requirements: This Investigator job family covers professional positions that conduct inspections in FDA regulated industries and prepare and submit reports accompanied by supporting evidence documenting violations of the FD&C Act and other laws, regulations, and requirements administered by FDA. The position investigates and/or inspects FDA-regulated industry globally and evaluates compliance with U.S. laws and regulations in order to promote a culture of safety and quality with the objective of preventing unsafe, ineffective and/or defective products from becoming available to patients and consumers or used in clinical trials while facilitating appropriate development of novel products. FDA's enforcement of the laws and regulations protects patients and consumers from products that are impure, unsafe, ineffective, improperly or deceptively labeled or packaged, or in some other way dangerous or defective. Investigators routinely examine products; collect samples; conduct inspections of establishments that design, make, process, hold, or distribute FDA-regulated products; and otherwise gather information and evidence to document objectionable conditions and assess compliance with U.S. law and regulations. Investigators apply critical thinking to evaluate manufacturing processes, design practices, facility and material controls, supply chains, quality management systems, laboratory analyses, and clinical investigation programs to assess compliance with U.S. laws and regulations and to support advancements and innovations. Investigators continuously maintain required certification and credentials; provide internal and external stakeholder outreach, assistance, and education; and may mentor less experienced personnel. These positions require knowledge of various scientific fields such as biochemistry, biology, biotechnology, chemistry, data science, digital health, engineering, epidemiology, food engineering, food processing technologies, food safety, healthcare, medical technology, microbiology, nutrition, pharmaceutical science, pharmacology, public health, quality assurance, and quality management. Education/Experience Requirement: Candidates must meet one of the following: Bachelor's degree in quality assurance/management, data science, statistics, computer forensics, epidemiology, pharmacy, public health, engineering, food science, law or regulations, or related healthcare or science field. The degree must be from an accredited program or institution AND two years of comparable experience with FDA, a state or federal partner agency, or in an FDA-regulated industry or organization providing investigative or compliance services to an FDA-regulated industry, focused on evaluating or ensuring compliance with FDA or related public health laws and regulations; -OR- Master's degree or higher in quality assurance/management, data science, statistics, computer forensics, epidemiology, pharmacy, public health, engineering, food science, law or regulations, or related healthcare or science field. The degree must be from an accredited program or institution AND one year of comparable experience with FDA, a state or federal partner agency, or in an FDA-regulated industry or organization providing investigative or compliance services to an FDA-regulated industry, focused on evaluating or ensuring compliance with FDA or related public health laws and regulations; -OR- Doctorate degree or higher in quality assurance/management, data science, statistics, computer forensics, epidemiology, pharmacy, public health, engineering, food science, law or regulations, or related healthcare or science field. The degree must be from an accredited program or institution; -OR- Four years of comparable experience with FDA, a state or federal partner agency, or in an FDA-regulated industry or organization providing investigative or compliance services to an FDA-regulated industry, focused on evaluating or ensuring compliance with FDA or related public health laws and regulations. Comparable experience is defined as experience with FDA, a state or federal partner agency, or in an FDA-regulated industry or organization providing investigative or compliance services to an FDA-regulated industry, focused on evaluating or ensuring compliance with FDA or related public health laws and regulations. NOTE: Applicants must submit all relevant transcripts that demonstrate you possess the required education to meet the Basic Qualifications. Become a part of the Department that touches the lives of every American. At the Department of Health and Human Services (HHS) you can give back to your community, state, and country, by making a difference in the lives of Americans everywhere! HHS is the principal agency for protecting the health of citizens. Join HHS and help to make our world healthier, safer, and better for all Americans. 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. The position is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Inspections and Investigations (OII), Office of Import Operations (OIO). The Office of Inspections and Investigations (OII) is at the forefront of building a public health safety net for today's complex, global regulatory environment. OII professionals work in a range of program areas and locations, with 196 offices throughout the United States." We need to extract substantive info and format. Let's create sections:

        About the role

        This position is being filled under a stream‑lined hiring authority under Title 21 of the United States Code (21 U.S.C. § 379d‑3a) as amended by the 21st Century Cures Act of 2016 (section 3072) and the Consolidated Appropriations Act of 2023 (section 3624). The selected candidate will serve under a career or career‑conditional appointment and be paid under the provisions of this authority, based on Title 21 Pay Table 1, Band A (GS‑11 equivalent). The role is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Inspections and Investigations (OII), Office of Import Operations (OIO). OII professionals work in a range of program areas and locations, with 196 offices throughout the United States.