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Prosidian Consulting

Management and operations consulting firm

Senior Quality Affairs SME - Healthcare and Life Sciences

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWashington, DC, USANo salary listed

About the Job

Requirements

  • At least 15 years of senior-level experience in quality assurance or quality control positions in the pharmaceutical industry.
  • Extensive knowledge and leadership experience in quality regulations and compliance.
  • Proven ability to manage high-level strategic quality planning for advanced development projects.
  • A degree in biology, chemistry, pharmacy, or a related scientific field, with commensurate quality assurance or control experience in the pharmaceutical or biotechnology industries.
  • Expertise in GXP compliance, including current Good Manufacturing Practice, Good Clinical Practice, and Quality System Regulations.
  • Ability to advise on and resolve critical quality issues at programmatic and project levels.
  • Ability to train and advise BARDA staff on compliance, regulations, and interactions with quality and manufacturing contacts.
  • Ability to manage quality regulations across vaccines, therapeutics, diagnostics, and medical devices.
  • Knowledge of government regulations, compliance frameworks, and regulatory engagement.
  • Proficiency with Microsoft Office tools; advanced skills with Excel, Access, Outlook, PowerPoint, and Word; proficiency with Adobe Acrobat, data analytic tools, and Visio; and ability to learn other tools as necessary.

Responsibilities

  • Support BARDA program offices as a subject-matter expert in chemical threats, radiological and nuclear threats, burn and blast injuries, biological threats, influenza, and emerging infectious diseases, and in research, development, manufacture, and regulatory approval, licensure, or clearance of medical countermeasures.
  • Provide guidance and recommendations on key issues in the relevant areas of expertise.
  • Serve as an advisor on Technical Evaluation Panels, including review of white papers, market research abstracts, technical proposals, and budget proposals.
  • Participate as a subject-matter expert on Program Coordination Teams.
  • Provide expert assessments, recommendations, guidance, and educational materials to Program Coordination Teams and Contracting Officer Representatives as needed.
  • Provide subject-matter expertise and advisory support to federal staff developing cost estimates for proposed programs or work.
  • Review and comment on study protocols, study reports, regulatory documents, presentations, proposals, and related documents.
  • Develop requested work products, including expert summary and opinion assessment reports, analysis reports, manuscript contributions, and reviews and technical assessments of solicitations, white papers, proposals, and post-award contract documents and deliverables.
  • Advise federal staff on the appropriateness and probability of success of contractor-proposed statements of work and recommend improvements.
  • Distill complex information into concise summaries, including risk-benefit analyses and balanced recommendations.
  • Participate in strategic discussions with the U.S. Government to build program areas aligned with BARDA’s mission.
  • Provide recommendations for project-development-level portfolio management and oversight as required.
  • Recommend or advise on developing, implementing, and improving Total Life Cycle Cost efforts, and participate in market research.
  • Provide expertise on quality assurance and control regulations across GXP frameworks supporting medical countermeasure development pathways.
  • Advise BARDA senior leadership on critical programmatic and project-level quality issues.
  • Train and advise BARDA staff on regulations, government compliance, and interactions with quality and manufacturing contacts at contract facilities.

Desired Qualifications

  • Experience in medicinal chemistry; preclinical development, including animal models, pharmacology, or toxicology; advanced clinical development, including medical officers, immunologists, or clinical operations; analytical product testing or test development; quality control; clinical or regulatory policy; manufacturing chemistry, manufacturing, and controls; process development, scale-up, or optimization; device development or manufacturing; reliability engineering; software; assay chemistry; microbiology; virology; immunology; or plastic consumable design and manufacturing.
  • Experience with manufacturing scalability and capacity expansion, sterile or aseptic techniques, sterile manufacturing or filling, and sterile facilities, including sterile gowning.

About the Company

Prosidian Consulting

Management and operations consulting firm

ProSidian Consulting is a management and operations consulting firm that helps private companies, Fortune 1000 enterprises, and government agencies solve problems and improve operations through tailored, industry-aligned services. It offers six enterprise practice areas: Risk Management, Energy & Sustainability, Compliance, Business Process, IT Effectiveness, and Human Capital, delivered by multidisciplinary teams across CONUS/OCONUS. The firm follows a structured approach to strategic solutions focused on growth, margin, and efficiency, aligning assets, processes, policies, and people to deliver value. With former Big 4 leadership and a nationwide/overseas footprint, its goal is to translate strategy into execution that boosts clients' return on invested capital and value delivered to customers.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Charlotte, NC
Founded
2008

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