PMO Technical Specialist

Frederick, MD
Full Time
Entry Level
PotomacWave is looking for a Project Management Office (PMO) Technical Specialist to join our team supporting a Federal client in Frederick, MD. This position provides support in priority areas such as systems engineering and compliance.  This is an excellent opportunity to learn different aspects of a PMO.  This position is currently working a hybrid schedule with two (2) days on-site per week. The ideal candidate will bring technical skills, analytical skills, an ability to maintain quality service standards, and great communication skills. 
 
Responsibilities:
  • Assist in the development of Capability Implementation Plans, which are based upon the guidance provided in DoD Instruction 5000.75.
  • Maintain and/or create required software, software licenses, and project IT hardware purchase agreements (credit card, contract, Service Level Agreements, etc.) to ensure the project’s operating capability is maintained/improved.
  • Prepare, coordinate, and conduct reviews for all determined program product modifications ensuring FDA compliance and system validations are maintained.
  • Develop change proposals to modify the implementation of the programs IT systems and capabilities.
  • Support and manage the development, implementation, and execution of Change Control activities for project/product maintenance. Coordinate with the Configuration Management team to ensure proper project planning and execution of initiatives.
  • Identify and establish necessary test/verification activities for the program office. Develop and maintain all required test/verification plans, procedures, and reports. Determine and coordinate all required test documentation.
  • Maintain system level validation for all products in accordance with the FDA (Title 21 CFR Part 11), as required, for all changes through appropriate testing, validation, and qualification procedures.
  • If other types of system level validation are required beyond the FDA requirements, ensure this is conducted for all changes through the appropriate testing, validation, and qualification.
  • Maintain all requirements within full compliance of FDA, DoD, Army, DHA, and/or other regulations and/or policies.
 
Qualifications:
  • One or more (1+) years of experience supporting IT, science, or clinical trials or related disciplines
  • Bachelor's Degree
  • Track record of producing quality deliverables
  • Strong organizational skills to be able to prioritize concurrent projects effectively and meet deadlines and commitments
  • Effective written and verbal communications, and positive interpersonal skills
  • Must have a Public Trust clearance or be a U.S. Citizen capable of obtaining a Public Trust clearance
Salary range $50,000 - $62,000
 

Equal Opportunity Employer/Race/Sex/Religion/Disability/Veteran Status/Sexual Orientation/Gender Identity/National Origin/Age.

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