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