Full-Time

Senior Quality Affairs SME

Prosidian Consulting

Prosidian Consulting

11-50 employees

Management and operations consulting firm

No salary listed

Washington, DC, USA

In Person

Category
Biology & Biotech (2)
,
Required Skills
Medicinal Chemistry
Microbiology
Pharmacology
Google Cloud Platform
Requirements
  • Degree in biology, chemistry, pharmacy, or related scientific fields
  • Commensurate experience in quality assurance/control in pharmaceutical or biotech industries
  • Expertise in GXP compliance (cGMP, GCP, Quality System Regulations)
  • Ability to advise on and resolve critical quality issues at programmatic and project levels
  • Strong communication skills to train and advise BARDA staff on compliance, regulations, and interactions with quality and manufacturing contacts
  • Strategic planning for QA/QC in medical countermeasure development
  • Knowledge of government regulations, compliance frameworks, and regulatory engagement
Responsibilities
  • Support BARDA Program Office(s) as a subject matter expert in the fields of Chemical Threats, Radiological/Nuclear Threats, Burn and Blast Injuries, or Biological Threats (including viral and bacterial threats), Influenza and Emerging Infectious Diseases Division (IEIDD) as well as the research, development, manufacture, and regulatory approval/ licensure/ clearance of medical countermeasures against these threats including but not limited to diagnostics and other medical devices/infrastructure vaccines and other preventives, and therapeutics.
  • Candidates with experience in medicinal chemistry; preclinical development (animal models, pharmacology, toxicology); advanced clinical development (medical officers immunologists, clinical operations); analytical product testing and testing development; quality control; clinical and/or regulatory policy; and/or manufacturing (chemistry, manufacturing, and controls); process development, process scale-up and process optimization; device development and manufacturing, reliability engineering, Software, Assay chemistry, microbiology, virology, immunology.
  • Provide guidance and recommendations on key issues related to the area(s) identified above.
  • Serve as advisor(s) on Technical Evaluation Panels (TEPs) to include white papers/market research abstracts, technical proposals, and budget proposals.
  • Participate as subject matter experts on Program Coordination Teams (PCTs)
  • Provide expert assessments, recommendations, and guidance as well as educational material to PCT and COR as needed
  • Provide subject matter expertise and advisory support to federal staff for development of cost estimates for notional programs/proposed work
  • Review and comment on study protocols, study reports, regulatory documents, presentations, proposals, and related documents.
  • Develop work products (including but not limited to expert summary reports, expert opinion assessment reports, analysis reports, manuscript writing/contribution, and review and technical assessments on a wide variety of documents related to BARDA’s mission, including solicitations, white papers, proposals, and post-award contract documents and deliverables), as requested in their SME area and at their required level of expertise.
  • Advise federal staff on the appropriateness and the probability of success of Contractor proposed statements of work Make suggestions on ways to improve those statements of work.
  • Experience distilling complex information into informative and concise summaries, including providing risk/benefit analyses and balanced recommendations.
  • Participate and aid in strategic discussions, working with USG, in building new program areas in alignment with BARDA’s mission space.
  • Provide recommendations for project development level portfolio management and oversight as required.
  • Provide recommendations or advise on development, implement, and consciously improve Total Life Cycle Cost (TLCC) efforts; Participate in Market Research efforts.
  • Provide subject matter expertise in quality assurance and control regulations in all GXPs supporting MCM development pathways.
  • Advise BARDA senior leadership on critical programmatic and project level quality issues.
  • Provide training and advisement to BARDA staff on regulations, compliance to government regulations, and interactions with quality and manufacturing contacts at contract facilities.
Desired Qualifications
  • At least 15 years of senior-level experience in QA/QC 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
  • Education in biology, chemistry, pharmacy, or related scientific fields
  • Commensurate experience in quality assurance/control in pharmaceutical or biotech industries
  • Expertise in government regulations, compliance frameworks, and regulatory engagement
  • Strong leadership in strategic quality planning and oversight
  • Ability to manage quality regulations across vaccines, therapeutics, diagnostics, and medical devices
  • Deliverables include work products related to cGMP regulations, GCP compliance, and Quality System Regulations
  • Involvement in strategic planning and guidance for BARDA's vaccine, therapeutic, and diagnostic programs
  • Advisory role in quality and compliance for advanced development and acquisition contracts
  • Provide subject matter expertise in quality assurance and control regulations for MCM pathways
  • Advise BARDA senior leadership on critical quality issues
  • Provide training on regulations, compliance, and interactions with manufacturing contacts
  • SmEs are expected to stay updated on evolving quality regulations and compliance frameworks
  • Ability to distill complex quality assurance/control issues into actionable guidance
  • High-level involvement in quality management for BARDA's strategic mission, including pandemic and emerging threat preparedness

ProSidian Consulting provides management and operations consulting to private companies, Fortune 1000 enterprises, and government agencies. It uses industry-aligned services across six practice areas: Risk Management, Energy & Sustainability, Compliance, Business Process, IT Effectiveness, and Human Capital, delivered by multidisciplinary teams. The firm connects strategy to execution with On-Demand Resources and targets drivers of economic profit—growth, margin, and efficiency—across assets, processes, policies, and people. Its goal is to help leaders design and execute operations that increase value for customers and improve return on invested capital.

Company Size

11-50

Company Stage

N/A

Total Funding

N/A

Headquarters

Charlotte, North Carolina

Founded

2008

Simplify Jobs

Simplify's Take

What believers are saying

  • Remote-first model attracts talent nationwide, cuts office overhead costs.
  • Energy & Sustainability practice meets tightening ESG mandates for Fortune 1000.
  • Human Capital solutions address 2025-2026 retention, skills gaps challenges.

What critics are saying

  • Deloitte poaches Big 4 alumni, erodes 190-professional talent pool in 6-12 months.
  • Stagnant website since 2020 loses clients to Booz Allen in 3-6 months.
  • No alliances post-2013 isolates energy bids against EY networks in 6-12 months.

What makes Prosidian Consulting unique

  • On-demand model deploys experienced-only Big 4 alumni for rapid execution.
  • Multidisciplinary teams span Risk Management, Energy & Sustainability, Compliance.
  • Structured approach links strategy to execution across assets, processes, people.

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Benefits

Remote Work Options