Voluntary Relocation Program **Vrp**

Department Of The Treasury San Francisco , CA 94118

Posted 4 days ago

  • Duties

HelpDuties Summary

WHAT IS THE VOLUNTARY RELOCATION PROGRAM (VRP)? The Voluntary Relocation Program (VRP) is a negotiated process which affords current Bargaining Unit employees the opportunity to relocate to a Post of Duty (POD) to a position that is the same as their home position of record, same grade, series and PD. Relocation must be an exact position match, the program does not allow for promotion or change to lower grades.

Learn more about this agency

Responsibilities

Applicants will ONLY be referred for positions that are same as their home position of record, same grade, series and PD. There is no promotion potential under the Voluntary Relocation Program. Applicants will ONLY be referred for locations which they wish to be considered. Applicants can request a copy of the position description if selected under this program.

Employees who apply after October 22,2018 will be considered following the next cutoff dates (July 22, 2019 through December 31, 2019). For more information, see Article 15, Section 6 of the 2019 National Agreement

WHERE CAN I FIND OUT MORE ABOUT OTHER IRS CAREERS? If you want to find out more about IRS careers, visit us on the web at http://www.jobs.irs.gov/

Supervisory status

No

Promotion Potential
00

  • Job family (Series)
    9999 Second Radio Electronics Technician

  • Requirements

HelpRequirements Conditions of Employment

  • Refer to other information.

  • Click "Print Preview" to review the entire announcement before applying.

  • Must be a U.S. Citizen or National.

  • IRS Employees on Career or Career Conditional Appointments.

  • Qualifications

You must meet the following requirements by the closing date of this announcement. You must have Exceeds Fully Successful or above on your last rating of record to be considered eligible under this program. All ratings will be verified at the time of application. Employees that have voluntarily moved under the Voluntary Relocation Program(VRP), received a new appointment or were competitively selected per the 2019 National Agreement Article 13 within the last two (2) years are not eligible under this program.

Education


upload resume icon
See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Associate Program Director Regulatory Program Management

Genentech

Posted 3 days ago

VIEW JOBS 1/17/2019 12:00:00 AM 2019-04-17T00:00 GENERAL POSITION SUMMARY/PURPOSE: In this key strategic role within the I2ON (immunology, infectious disease, ophthalmology, neuroscience) Genentech Regulatory Program Management team you will formulate US and global regulatory strategies drawing on your own expertise and the resources of the global Roche regulatory network to drive product development from early development to post-marketing. You will take the lead for assigned projects and represent PDR to cross-functional teams and groups and serve as the principal interface with health authorities, developing the strategies for, managing, and executing these interactions. Genentech, a member of the Roche group, has one of the richest and most diverse pipelines in the industry. The entrepreneurial spirit and inventiveness of our founders still defines our culture; a culture that encourages innovation and bold steps as vital partners to rigorous science. As you set off on the next leg of your regulatory career journey, explore Roche. Go ahead. Make a change. Make a difference. PRIMARY DUTIES AND RESPONSIBILITIES: * Plays a key role in creating innovative long-range strategies to expedite development of our projects in immunology, infectious disease, ophthalmology, or neuroscience therapeutic areas from entry into man through lifecycle management. Although the therapeutic area may evolve over time, currently, this position is expected to be the regulatory leader for two early development asthma projects. * Develops regulatory strategies with global cross functional clinical, non-clinical and business teams. Provides project teams with leadership regarding regulatory authority interactions. * As the US regulatory subject matter expert, leads the US Regulatory strategy as a member of a global Regulatory Affairs Functional Team (RAFT) for assigned development projects. Depending on your project assignment, you will also serve as the primary regulatory lead on one or more regional or global projects at any one point in time and be the regulatory read of the RAFT. * Acts as primary liaison and manages a professional relationship between the FDA and project teams for assigned projects. * Responsible for on time and quality regulatory submissions for INDs and BLAs/NDAs to the FDA. * Collaborates with the Canadian regulatory affiliate to develop and manage regulatory strategy and submissions to Health Canada for assigned projects. * Briefs regulatory management * Mentors and coaches junior regulatory professionals. * Stays abreast of internal and external developments, trends and other dynamics relevant to the work of Product Development and Regulatory to maintain, at all times, a fully current view and perspective of internal/external influences and/or implications for assigned therapeutic areas and projects. * Continues to expand his/her knowledge base of laws, regulations and guidelines governing the development, licensure and marketing of drugs and biologics. QUALIFICATIONS & EXPERIENCE: * Bachelor's Degree required (life sciences disciplines strongly preferred) * Average of 5 or more years' relevant experience in regulatory affairs or related functions in drug/biologics development/manufacturing. Experience participating in global product development teams is preferred. Experience in development of products to treat respiratory diseases, such as asthma, a plus. * Experience as a regulatory contributor for global original IND/NDA/BLA filings in the US is preferred. * Broad understanding of US FDA regulations, processes and issues in drug/biologics development. Includes in-depth knowledge of GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use). * Previous experience working in a matrix management environment. #LI-PDAB1 Genentech South San Francisco CA

Voluntary Relocation Program **Vrp**

Department Of The Treasury