Food and Drug Administration Logo
Position Title
Consumer Safety Officer
Agency
Food and Drug Administration
Announcement Number
FDA-ORA-23-IMP-11884451-WM Opens in new window
Open Period
Thursday, March 16, 2023 to Wednesday, March 29, 2023
For preview purposes only. To apply, please return to the USAJOBS announcement and click the Apply button.
Eligibilities
1. PLEASE READ THE FOLLOWING MERIT PROMOTION ELIGIBILITY QUESTIONS VERY CAREFULLY.
Your responses to these questions will impact your eligibility.

This vacancy announcement is being advertised under Merit Promotion procedures. This means that only specific groups of applicants are eligible to apply to this announcement. The following eligibility questions will determine if you are among any of these specific groups eligible to apply. You will only be considered for each eligibility which you respond "yes" to. If you respond "no" to all eligibility options in this list, your application will not be considered under this advertisement. For more information about Merit Promotion advertisements, visit the USAJOBS Which Vacancies am I Eligible For? article. The specific area of consideration (those groups of applicants eligible to apply) are listed in the "Who May Apply" section of this announcement. If you still have questions about this advertisement or your potential eligibility, please reach out to the FDA Applicant Help Desk | quickquestions@fda.gov | 888-478-4340.
By answering "yes" below, you are indicating that you have read and understand this information.
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2. Are you a current employee of any agency within the Department of Health & Human Services (HHS) who has been notified that your job is no longer needed or that you will lose your job by Reduction-in-Force (RIF)? If so, you may be entitled to selection priority under the Career Transition Assistance Plan (CTAP).

To be eligible, you must:
1. Meet the definition of 'surplus' or 'displaced' employee, as defined in Section 330-2-30; and
2. Have a duty station in the local commuting area of the vacancy; and
3. Have a performance rating of at least Fully Successful or equivalent; and
4. Be applying to a position that is at or below the grade level of the position from which you're being separated; and
5. Be applying to a position that does not have greater promotion potential than the position from which you're being separated; and

6. Be well-qualified for the position. Refer to the vacancy announcement for a description of the criteria; and
7. Submit the following supporting documentation:
  • RIF separation notice or a Proposed Removal/Separation notice; and
  • Copy of your latest performance rating; and
  • Copy of your most recent SF-50: Notification of Personnel Action showing your position, grade and step, tenure code, and duty location.
See the Career Transition Assistance site on USAJOBS for more information about CTAP.
Based on the above, are you eligible and would you like to be considered for selection priority under the Career Transition Assistance Plan (CTAP)?


 
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3. Are you a current Food and Drug Administration (FDA) employee? If so, you may be eligible to apply competitively to this vacancy announcement.
To be eligible, you must:
1. Be a current permanent FDA employee on a career or career-conditional in the competitive service. If you are unsure, review your SF-50: Notification of Personnel Action for the following:
  • Block 24 (Tenure) must be '1 - Permanent' or '2 - Conditional'; and
  • Block 34 (Position Occupied) must be '1 - Competitive Service'
AND
2. Have never held a permanent position with the same or greater promotion potential. Review the vacancy announcement for the promotion potential of this position.
AND
3. Submit a copy of your most recent SF-50: Notification of Personnel Action with your application package. Review the Required Documents section of the vacancy announcement.
Based on the above, are you eligible and would you like to be considered as a current FDA employee (Competitive)?
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4. Are you a current Food and Drug Administration (FDA) employee? If so, you may be eligible to apply non-competitively to this vacancy announcement.
To be eligible, you must:
1. Be a current permanent FDA employee on a career or career-conditional appointment in the competitive service. If you are unsure, review your SF-50: Notification of Personnel Action for the following:
  • Block 24 (Tenure) must be '1 - Permanent' or '2 - Conditional'; and
  • Block 34 (Position Occupied) must be '1 - Competitive Service'
AND
2. Currently hold or have previously held a permanent position with the same or greater promotion potential. Review the vacancy announcement for the promotion potential of this position. You must submit a copy of your SF-50: Notification of Personnel Action showing the highest grade (or promotion potential) held.
AND
3. Submit a copy of your most recent SF-50: Notification of Personnel Action with your application package. Review the Required Documents section of the vacancy announcement.
Based on the above, are you eligible and would you like to be considered as a current FDA employee (Non-Competitive)?
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5.
  • Are you a current HHS employee in a bargaining unit position represented by the National Treasury Employees Union (NTEU)? NOTE: This question is not used to determine if you are eligible for consideration; it is only used to ensure proper referral in accordance with the HHS and NTEU collective bargaining agreement effective October 1, 2010, revised March 6, 2014. Therefore, in order to be considered for this position, you must also respond "Yes" to the applicable eligibility questions below.
    If you answer yes, Block 37 (Bargaining Unit Status) of your SF-50 must be 3591.
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6.
Are you a current Public Health Service (PHS) Commissioned Corps Officer stationed at a position within the Food and Drug Administration (FDA)? Not all positions are appropriate for the Commissioned Corps and it is at the supervisor's discretion to fill a position through the Corps.
To be eligible, you must:
1. Be a current PHS Commissioned Corps Officer with FDA; and
2. Submit a copy of your most recent PHS personnel orders or letter from the Public Health Service verifying you are currently in, or have been accepted to, the Commissioned Corps.
See the PHS Commissioned Corps website for more information.
Based on the above, are you eligible and would you like to be considered for a Commissioned Corps appointment?
 
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7. Position requires driving to various job sites using private vehicles or government owned vehicles. Do you have a valid driver's license? (limit characters)
Preferences
1. Select the location(s) you want to be considered for. You must choose at least one location. You may only select up to 1 location(s). (limit characters)
2. In the last five years, based on the closing date of this announcement, have you served or are you currently serving as an Executive Branch political, Schedule C, or Non-career SES appointee?
You can find out if you have held one of these appointment types by looking at your Standard Form 50s in your Electronic Official Personnel Folder (eOPF), in Section 5 where the legal authorities are listed.
  • A political appointee is an appointment made by the President without confirmation by the Senate (5 CFR 213.3102(c)) OR an assistant position to a top-level federal official if filled by a person designated by the President as a White House Fellow (5 CFR 213.3102(z)).
  • A Schedule C appointee occupies a position excepted from the competitive service by the President, or by the Director of OPM, because of the confidential or policy-determining nature of the position duties (5 CFR 213.3301 and 5 CFR 213.3302).
  • A Non-career SES appointee is approved by the White House and serves at the pleasure of the appointing official without time limitations (5 CFR 317 Subpart F).
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3.

===== Acknowledgement of Restrictions on the Employment of Relatives by Public Officials =====
5 U.S. Code, § 3110 lays out specific and important restrictions on the employment of relatives within an agency.
A public official of a government agency may not appoint, promote, or otherwise advocate for the employment, advancement, or promotion of relatives within the agency for which the public official is employed or has control over.
Employees hired in violation of 5 U.S. Code, § 3110 will not be entitled to any pay for their period of employment, and any pay already received before the violation becomes known, will be considered as a debt to the government on the part of the employed individual.

For the purpose of this question, a "relative" is defined as: father, mother, son, daughter, brother, sister, uncle, aunt, first cousin, nephew, niece, husband, wife, father-in-law, mother-in-law, son-in-law, daughter-in-law, brother-in-law, sister-in-law, stepfather, stepmother, stepson, stepdaughter, stepbrother, stepsister, half brother, or half sister.

QUESTION:
After having read the definition of "relative" as stated above, does the Food and Drug Administration employ any of your relatives?

IF YES: You must provide the following information, for each relative employed by the FDA:

  1. The full legal name of the relative.
  2. The relative's relationship to you (from the list above).
  3. If known, the relative's employing organization and position.
IF NO: Please type "No" in the box below.
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4. Your responses to the all questions, and any information or documentation which you provide as part of your application, will be thoroughly reviewed for accuracy and truthfulness. Please take this opportunity to review your responses to ensure their accuracy. If you fail to answer this question, your application will not be considered. Knowingly providing false information in your application (or submitted documentation) is a crime!
  1. I certify that, to the best of my knowledge and belief, all of the information included in my application is true, correct, and provided in good faith.
  2. I understand that if I intentionally make a false statement, or commit deception or fraud in my application, or in any document or interview associated with the examination process, I may be fined or imprisoned (18 USC, Sec 1001); my eligibility may be canceled, I may be denied an appointment, or I may be removed and debarred from Federal service (5 CFR, Part 731).
  3. I understand that any information I provide may be investigated.
  4. I understand that responding "No" to this item will result in my not being considered for this position.
Do you accept the conditions above?
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Assessment 1
We will evaluate your resume and your responses to this Assessment Questionnaire to determine if you are among the best qualified for this position. Your responses are subject to verification. Please review your responses for accuracy before you submit this questionnaire.
 
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1. From the description below, select the one which best describe your position.
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2. From the description below, select the one which best describes your education and/or experience and meets the Basic Qualification Requirements for GS-0696, Consumer Safety Officer. To be found qualified; your resume and/or transcripts MUST support the response that you select.
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3. From the description below, select the one which best describes the experience you possess that demonstrates your ability to perform the duties of a Consumer Safety Officer, GS-0696-13 position. To be found qualified; your resume MUST support the response that you select.
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Select the one statement that most accurately describes your training and experience carrying out each task using the scale provided. (limit characters)
4. Make recommendations to management officials as to whether or not a firm/individual is in compliance with Current Good Manufacturing Practices (CGMP). (limit characters)
5. Review reports of inspections and investigations for violations and determine the sufficiency of the evidence. (limit characters)
6. Manage the review of previously approved products to determine whether they should continue to be permitted in light of current scientific safety criteria. (limit characters)
7. Coordinate the collection of data, manage the scientific review and recommend a course of action. (limit characters)
8. Conduct the more complex, technical investigations and inspections of both domestic and international establishments. (limit characters)
9. Investigate and evaluate the adequacy of complex manufacturing practices to determine compliance with GMP regulations. (limit characters)
10. Perform investigations involving complaints of injury or death attributable to products regulated by the FDA. (limit characters)
11. Plan and decide how the investigation should proceed, when the investigation is complete, and what reporting is required. (limit characters)
12. Assess risk of human food manufacturing or farming problems. (limit characters)
13. Serve on task forces and study groups charged with considering problems or directions in the area of food programs. (limit characters)
14. Consult with staff members at all levels of the organization to achieve consensus on issues and resolve any disagreements on standards. (limit characters)
15. Represent the agency on inter-agency review committees charged with reviewing Federal policies and making recommendations for consistency across agency lines. (limit characters)
16. Meet with industry representatives to exchange information to provide advice and guidance. (limit characters)
17. Serve as an expert witness in area of expertise in court cases dealing with regulated products. (limit characters)
18. Prepare memoranda, briefings, and other background material concerning substantive issues, findings, and conclusions and propose solutions to keep the appropriate staff involved at key decision points. (limit characters)
19. Review reports and publications for relevant information. (limit characters)
20. Organize, analyze and summarize information on reports. (limit characters)
21. Prepare proposed or final EIR endorsements or corrective action because of inspection. (limit characters)
22. Conduct on-the-job and other training for staff other personnel regarding technical and scientific matters, inspectional/investigational issues, policies, and laws
affecting the food program area.
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23. Serve as a principal advisor or team leader in a field of regulatory and compliance expertise. (limit characters)
24. Plan, coordinate and evaluate programs and activities for a professional regulatory field. (limit characters)
25. Make field decisions on the nature and extent of follow-up investigations. (limit characters)