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Senior Biopharmaceutical Scientist Security Clearance

Job in McLean, Fairfax County, Virginia, USA
Listing for: MITRE Corporation
Full Time position
Listed on 2026-06-18
Job specializations:
  • Science
    Medical Science, Research Scientist
Job Description & How to Apply Below
Position: Senior Biopharmaceutical Scientist with Security Clearance
Why choose between doing meaningful work and having a fulfilling life? At MITRE, you can have both. That's because MITRE people are committed to tackling our nation's toughest challenges-and we're committed to the long-term well-being of our employees. MITRE is different from most technology companies. We are a not-for-profit corporation chartered to work for the public interest, with no commercial conflicts to influence what we do.

The R&D centers we operate for the government create lasting impact in fields as diverse as cybersecurity, healthcare, aviation, defense, and enterprise transformation. We're making a difference every day-working for a safer, healthier, and more secure nation and world. Our workplace reflects our values. We offer competitive benefits, exceptional professional development opportunities for career growth, and a culture of innovation that embraces adaptability, collaboration, technical excellence, and people in partnership.

If this sounds like the choice you want to make, then choose MITRE - and make a difference with us.

Department Summary:

MITREs Biotechnology and Life Sciences Department is a mission-focused scientific department dedicated to advancing pharmaceutical solutions that support U.S. defense and public health preparedness objectives. The department provides technical expertise accelerate the delivery of safe, effective Medical Countermeasures and ensure resilient pharmaceutical supply chains. Working across multidisciplinary teams, we support rapid development, technical problem-solving, and transition of drug products to meet operational, emergency response, and national security needs.

Roles & Responsibilities :
We are seeking an experienced Senior Pharmaceutical Scientist to lead the development of small molecule drug products supporting advanced research, development, manufacturing, and lifecycle management activities. This role will provide technical and strategic leadership across formulation development, process development, analytical characterization, manufacturing support, and supply chain resilience for orally delivered, injectable, topical, or other small molecule prophylactic and therapeutic products.

The ideal candidate will bring expertise in small molecule pharmaceutical development and experience supporting Medical Countermeasures programs aligned with the mission needs of the U.S. Government, including candidate assessment, preclinical development, clinical-stage development (including under the animal rule), manufacturing, and transition to sustainment of products intended to address operational, emergency preparedness, and national security requirements.
* Develop and evaluate technical and programmatic strategies for developing small molecule pharmaceutical products from preformulation through clinical and commercial readiness

* Provide subject matter expertise related to formulation development, excipient compatibility, process scale-up and optimization, stability, dissolution, bioavailability, manufacturability, quality, and analytical method development for small molecule drug candidates

* Support development of pharmaceutical products intended to meet Medical Countermeasures needs of the U.S. Department of War, including products relevant to force health protection, emergency response, and operational readiness

* Investigate supply chain dependencies, bottlenecks, and chokepoints to inform U.S. strategies and programs to establish and sustain resilient pharmaceutical supply chains.

* Provide technical leadership for drug product development activities involving tablets, capsules, suspensions, solutions, lyophilized products, injectables, or other small molecule dosage forms including combination products

* Collaborate with cross-functional teams in R&D, manufacturing, quality, regulatory, clinical, and program management to advance small molecule development programs

* Identify, assess, and develop mitigation strategies for technical, business, and programmatic risks to medical countermeasure development

* Analyze complex data to support formulation selection, process robustness, product quality, and shelf-life determination

* Author and review technical reports, development plans, study protocols, specifications, validation documents, deviation investigations, and regulatory submission content

* Support scale-up, process transfer, and manufacturing readiness activities for pilot, clinical, and commercial production

* Ensure work is conducted in compliance with applicable regulatory and quality standards, including cGMP, GLP, FDA regulations and guidance, and ICH guidelines

* Serve as a trusted advisor to U.S. Government Sponsors.

* Monitor scientific, regulatory, and industry trends relevant to small molecule therapeutics, pharmaceutical technologies, and defense-focused Medical Countermeasures programs

Basic Qualifications:

* MS + 5 years of experience or Ph.D. +3 years of experience in Pharmaceutical Sciences, Chemistry, Medicinal Chemistry, Chemical…
Position Requirements
10+ Years work experience
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