Bioengineer IV

Please note that this position is contingent upon the successful award of a contract currently under bid.

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 IV shall provide technical, scientific, and programmatic support to the CTO Program Office and project teams, providing advice and assistance for advanced development efforts (i.e., clinical, non-clinical, and manufacturing) related to CBRN threats.

Essential Job Functions:

• The contractor shall assist with Government oversight of development contractor efforts, to include conducting site visits, assisting in monitoring performance and quality standards, and providing technical oversight.
• The contractor shall conduct data analyses and create and submit study results to use in market research or publications. The contractor shall develop and/or review technical documentation.
• The contractor shall provide program office support and participation at conferences and stakeholder meetings.
• The contractor shall participate in internal and external IPTs, to include organizing meetings, preparing agendas, and documenting meeting minutes and action items.
• The contractor shall draft reports, to include executive summaries, significant actions, manuscripts, and other technical documents (e.g., technology transition agreements, concept transition agreements, requests for proposals, statements of work, etc.).
• The contractor shall research and review scientific literature and databases to identify technical information and provide references to support product development efforts.
• The contractor shall review scientific data, reports, and technical submissions.
• The contractor shall effectively communicate results of assigned tasks and efforts, both orally and in written form, in a clear and concise manner, to include executive summaries, meeting presentations, documentation, and reports.
• The contractor shall deliver written work products no later than the assigned suspense (which will be earlier than those established by external sources (e.g., SASI, DSS, higher headquarters suspense dates, etc.) to allow for Government review, revision, and coordination prior to Government approval and submission).
• The contractor will be required to write reports and briefs.
• The contractor will be required to review the reports and briefs of other agencies.
• The contractor shall build and maintain relationships with contract performers and establish periodic meetings to communicate performance issues and concerns to reduce risk to the program on a quarterly basis.

Necessary Skills and Knowledge:

• Shall possess a strong understanding of relevant literature and be able to effectively debate highly technical issues with other government and contractor experts.
• The contractor shall possess five (5) years of working experience with Microsoft Office, to include Outlook, Project, PowerPoint, Excel, and Word.
• The contractor shall possess familiarity with nonclinical studies, ordering and procuring nonhuman primates, including study points and implementation of Good Laboratory Practices (GLP) (21 Code of Federal Regulations (CFR) 58) toxicity studies and US FDA Animal Rule (21 CFR 314.600 and 601.90) studies to evaluate efficacy of biodefense pharmaceuticals.
• The contractor shall possess an understanding of pre-clinical and clinical drugs, biologics, or assays advanced development (IND to FDA licensure).

Minimum Qualifications:

• Master's degree in Chemistry, Biology, or a related discipline, as well as five (5) years of general experience and two (2) years of relevant experience.
  • Tradeoff Requirement: Possess Bachelor's degree in Chemistry, Biology, or a related discipline, as well as ten (10) years of general experience and five (5) years of relevant experience.
• Minimum five (5) years of Industry experience in pharmaceutical/biotechnology advanced development (IND to FDA approval). The contractor shall possess experience in program management, product development, acquisition program strategic planning, contract guidance, oversight, and advisory services.
• Clearance: Secret

Pay and Benefits

The salary range for this position is $120,000 to $160,000 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.