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Bioengineer III - Clearance Required

Job Locations US-MD-Fort Detrick
Posted Date 2 months ago(6/28/2024 10:05 AM)
Job ID
2024-11524
# of Openings
3
Category
Engineering

Overview

LMI is seeking a qualified Bioengineer III to support our Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear (JPEO-CBRND) Joint Project Manager for Medical Countermeasure Systems (JPM MCS) client at our Ft. Detrick, MD location. Active Secret clearance preferred; only candidates eligible for a Secret level clearance will be considered (US Citizenship required).
 
LMI is a consultancy dedicated to improving the business of government, drawing from deep expertise in advanced analytics, digital services, logistics, and management advisory services. Established as a private, not-for-profit organization in 1961, LMI is a trusted third party to federal civilian and defense agencies, free of commercial and political bias. We operate completely free of political and commercial bias, and we are entirely aligned with the goals of our clients. Our clients value our specialized services in logistics, intelligence, homeland security, health care, and energy and environment markets. We believe government can make a difference, and we seek talented, hardworking people who share that conviction. We offer a generous compensation package with excellent benefits that start the first day of employment. Business casual dress, flex time, and tuition reimbursement are a few of our many work-life benefits available to our employees.

Responsibilities

  • Serve as the Assistant to the Vaccine Manager on project teams, supporting risk planning efforts and providing advice and assistance in implementing process improvements for advanced development efforts (i.e., clinical, non-clinical, and manufacturing).
  • Serve on internal and external IPTs, responsible for organizing meetings, preparing agendas, documenting meeting minutes and action items, and maintaining the document archive system.
  • Provide written technical opinions to guide the decision-making process of the IPT.
  • Participate in contractor site visits, assisting in monitoring performance, regulatory and quality standards, and providing technical oversight during study execution.
  • Serve as the programmatic representative at conferences and stakeholder meetings.
  • Provide scientific/technology advice, technical oversight, and project management support in the areas of science and technology availability, technology maturity, and applicability of proposed candidate CBRN medical countermeasures through advanced development, DoD acquisition processes, production, and fielding.
  • Provide technical knowledge to guide the product team in establishing a link between clinical and non-clinical efficacy, developing a robust manufacturing strategy, and defining product development schedules.
  • Collaborate with project teams and participate in the evaluation of technical results in multiple developmental areas, developing strategies to move the program forward.
  • Collaborate with both internal and external partners, contributing to data analyses in order to create and submit study results to publications or the FDA.
  • Provide periodic update reports to PMs.
  • Assist the PMs in assessing cost and schedule risks and developing mitigation strategies.
  • Draft and/or review acquisition documentation and presentations in support of major milestones, program reviews, or other program presentations.
  • Develop drafts and/or review and provide edits/comments to technical documentation (i.e., development/technology transfer reports, batch records, standard operating procedures, and regulatory submissions).
  • Author, edit, and contribute to the development of robust product development plans to support FDA approval under the Animal Rule.

Qualifications

  • Standard Requirement: Master’s degree in Engineering, Physics, Chemistry, Biology, Engineering Management, or a related discipline, as well as eight (8) years of general experience and five (5) years of relevant experience.
  • Tradeoff Requirement:  Bachelor’s degree in Engineering, Physics, Chemistry, Biology, Engineering Management, or a related discipline, as well as ten (10) years of general experience and seven (7) years of relevant experience.
  • DAU Level II equivalency in Program Management or senior-level DoD experience in pharmaceutical/biotechnology vaccine and drug development portfolio management (i.e., investment decisions based on the risk management process). The contractor shall possess five (5) years of Industry experience in pharmaceutical/biotechnology advanced development (i.e., IND to FDA approval).
  • Five (5) years of project management experience in cost, schedule, performance, risk analysis, and advice.
  • Strong analytical and problem solving skills, as well as good organization skills to balance and prioritize work.
  • Extensive customer support/relations experience.
  • Strong interpersonal and communication skills, both oral and written.
  • Capable of maintaining interpersonal contacts to increase effective team dynamics; effectively communicating ideas, requirements, and scientific knowledge across and within organizations united for the development of medical countermeasures.
  • Five years of working experience with Microsoft Office, to include Outlook, Project, PowerPoint, Excel, and Word.
  • Active Secret clearance preferred; only candidates eligible for a Secret level clearance will be considered (US Citizenship required).

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LMI is an Equal Opportunity Employer. LMI is committed to the fair treatment of all and to our policy of providing applicants and employees with equal employment opportunities. LMI recruits, hires, trains, and promotes people without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, pregnancy, disability, age, protected veteran status, citizenship status, genetic information, or any other characteristic protected by applicable federal, state, or local law. If you are a person with a disability needing assistance with the application process, please contact accommodations@lmi.org
Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

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