Enter your Social Security Number in the space indicated. Your Social Security Number is requested under the authority of Executive Order 9397 to uniquely identify your records from those of other applicants who may have the same name. As allowed by law or Presidential directive, your Social Security Number is used to seek information about you from employers, schools, banks and others who may know you. Providing your Social Security Number is voluntary, however we can not process your application without it.
Are you a PHS Commissioned Officer (This includes active duty officers, inactive reserve officers, and applicants who have been approved for commissioning in the USPHS Commissioned Corps)?
Enter the lowest grade level that you will accept for this position. The lowest grade for this position is 13.
Select/enter at least one occupational specialty. The specialty code for this position is:
Choose 001 Merit Promotion if you have not held a permanent position at the grade level(s) posted in this vacancy announcement.
Choose 002 - Reassignment or Non-Competitive Promotion if on a permanent basis, you currently hold or have previously held a position at the grade level(s) posted on this vacancy announcement and the position had promotion potential to the GS-13 grade level or above. OR I am a current FDA/ORA Commissioned Corps Officer; OR I am a current FDA/ORA employee serving under the SCHA appointment.
Select/enter at least one geographic location in which you are interested and will accept employment. The location code for this position is:
Please answer yes or no to statement one. Your response will determine if you are qualified for the GS-0696-13, Consumer Safety Officer (Devices) position.
1. I have at least one year of specialized experience that has equipped me with the particular knowledge, skills and abilities to successfully perform the duties of the position. This experience is related to the work of the position and equivalent to at least the GS-12 level in the Federal service as described in the vacancy announcement.A. Yes
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.A. I have a degree that included at least 30 semester hours in one or a combination of the following: biological sciences, chemistry, pharmacy, physical sciences, food technology, nutrition, medical science, engineering, epidemiology, veterinary medical science, or related scientific fields that provided knowledge directly related to consumer safety officer work. The 30 semester hours can include up to 8 semester hours in statistics, or course work that included the principles, theory, or practical application of computers or computer programming.
Please answer yes or no to the statement below. Your response will determine if you meet the time-in-grade requirement for this position.
I have 52 weeks at the GS-12 grade level or above in the Federal Service within 30 days of the closing date of the announcement.A. Yes
Your response to the statement below will determine if you meet the area of consideration.
4. I am a current employee of the Food and Drug Administration, Office of Regulatory Affairs OR I am a current FDA-ORA Commissioned Officer OR I am a current FDA/ORA employee serving under the SCHA appointment.A. Yes
Your response to the statement below will determine if you are eligible for non-competitive referral.
5. Please select the appropriate response from the list below.A. I am currently serving in a permanent position at the GS-13 grade level or above in the Federal Service.
For each task in the following group, choose the statement from the list below that best describes your experience and/or training. Darken the oval corresponding to that statement in Section 25 of the Qualifications and Availability Form C. Please select only one letter for each item.
Note: Submission of this electronic questionnaire is certification that all responses are true to the best of your knowledge. Materially false, fictitious, or fraudulent statements or representations are subject to disciplinary action.
6. Serve as an expert in inspectional and investigative techniques and technical knowledge in GMP inspections of various medical device manufacturers.
7. Conduct international GMP inspections covering medical devices.
8. Serve as expert in terms of inspectional/investigative procedures and developing evidence when situations are encountered that may result in regulatory action.
9. Serve as an expert, research and resolve recurring problems of national and international scope encountered by other Field Offices or other Regions.
10. Work with a complex category of products or a functional specialty pertaining to medicine, science, and/or technologies involving legal, regulatory, and diplomatic concepts necessary to enforce the laws.
11. In-depth knowledge of a category of products or a functional specialty which is distinctly more difficult to work with because of the medicine, science, and/or technologies involved and because the legal, regulatory, and diplomatic concepts necessary to enforce the law are correspondingly more complex and/or unprecedented.
12. Perform complex assignments in the international arena which require extensive scientific knowledge of the particular industry practices accumulated by experience in investigations and inspections.
13. Consult and participate in the formulation and developing of inspectional and investigational procedures and techniques.
14. Ability effectively negotiate and resolve issues in sensitive situations arising in highly complicated assignments.
15. Communicate agency requirements, policies and procedures.
16. Interact, routinely and coordinate with foreign governments.
17. Provide testimonial presentations used as instruments for negotiations; conduct negotiations with industry representatives and other government agencies.
18. Prepare and propose endorsements with an inspection conclusion and district decision.
19. Prepare written reports, findings, and recommendations; develop analyses that are used for disposition of cases and formal training programs.
20. Review drafts and proposals pertaining to the promulgating of regulations making analyses if such are feasible or desirable.