Bioengineer Level: V at Goldbelt, Inc.

Frederick, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Aug, 26

Salary

0.0

Posted On

15 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Program Management, Product Development, Acquisition Strategic Planning, Contract Oversight, Regulatory Applications, Portfolio Management, Risk Management, Microsoft Project, Microsoft Excel, Drug Development Process, Cost Analysis, Schedule Analysis, Performance Analysis, Customer Relations, Problem Solving, Organizational Skills

Industry

Health and Human Services

Description

Overview Goldbelt Professional Services specializes in providing expert resources for Public Health missions including scientific, technical, and administrative support from junior staff to high-level subject matter experts. Research and data driven, Goldbelt Professional Services’ experts create solutions customized to the client’s needs. Summary: The Bioengineer Level: V will serve as the primary programmatic representative on project teams, providing project management support and strategic advice for the advance development of CBRN medical countermeasures. Assist Project Managers in assessing cost, schedule, and performance risks, and take the lead in developing and implementing mitigation strategies. Lead the drafting, reviewing, and editing of acquisition documentation, including Statements of Work (SOWs), development plans, and presentations for program reviews. The JPEO-CBRND manages our nation's investments in chemical, biological, radiological, and nuclear defense equipment, and medical countermeasures. Battlespace worldwide. JPM CBRN Medical consists of the following product development organizations: Chemical Defense Pharmaceuticals (CDP): Provides the warfighter and the nation with robust and affordable U.S. Food and Drug Administration (FDA)-approved lifesaving MCMs against CBRN threats. CDP plays a critical and strategic role in chemical defense by providing the warfighter with protect-and-mitigate capabilities against known or novel threats. Responsibilities Essential Job Functions: Extensive expertise in program management, product development, acquisition program strategic planning, and contract oversight. Industry & Regulatory, serving as a Program Manager, Director, Principal Investigator, or team lead within a commercial pharmaceutical or biotechnology company, managing the development and filing of regulatory applications (e.g., IND, BLA, NDA, 510(k)). Portfolio Management experience in pharmaceutical/biotechnology portfolio management, including making investment decisions based on a formal risk management process Scheduling & Financials demonstrate proficiency with Microsoft Project and Excel for managing resource-loaded Integrated Master Schedules (IMSs) and financial documents Technical Acumen and strong understanding of the drug /biologic/diagnostic development process (from IND to FDA licensure) to effectively manage and oversee technical teams and debate issues with subject matter experts. Qualifications Necessary Skills and Knowledge: Project Management Experience: at least five (5) years of direct project management experience, demonstrating mastery in cost, schedule, performance, and risk analysis and mitigation. Communication: must have extensive customer support/relations experience and strong analytical, problem-solving, and organizational skills. Minimum Qualifications: Master's degree in relevant scientific or engineering discipline (Engineering, Physics, Chemistry, Biology, Engineering Management, Pharm D, Virology, Microbiology, Molecular Biology, Biochemistry, Biochemical Engineering) with eight (8) years of relevant experience and five (5) years of relevant experience, OR a Bachelor's degree with a minimum of ten (10) years of relevant experience in managing complex technical programs Clearance: Secret PREFFERED QUALIFICATIONS (education, experience, skills) Certification in Program Management (e.g., PMP) - Highly Desired DAU Level I (or higher) equivalency in Program Management Project Scheduling Professional Certification Experience aligning FDA processes with acquisition requirements for medical product development. Pay and Benefits The salary range for this position is $155,000 to $165,000 annually. At Goldbelt, we value and reward our team's dedication and hard work. We provide a competitive base salary commensurate with your qualifications and experience. As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan with company matching, tax-deferred savings options, supplementary benefits, paid time off, and professional development opportunities.

Responsibilities

Serve as the primary programmatic representative providing project management and strategic advice for CBRN medical countermeasure development. Lead the drafting of acquisition documentation and manage cost, schedule, and performance risks.