Technical Advisor, Advanced Supply Chain Solutions ( Fixed Term)

US Pharmacopeia; Rockville (MD); On-site; USD 126,000 - 177,000; Full time

Job summary

USP seeks a scientific and technical expert for a two-year fixed-term Technical Advisor role. You will evaluate APIs, KSMs, and related supply chains, translating complex data into actionable, evidence-based recommendations.

You will collaborate with chemists and data scientists to deliver high-quality deliverables across donor-funded projects and timelines.

Qualifications

• Ph.D. in Organic Chemistry with 2+ years of industrial API/fine chemical experience.
• Demonstrated scientific and technical writing experience.
• Experience conducting literature searches, database reviews, and evidence synthesis.
• Strong analytical and communication skills.
• Ability to work independently and in a matrixed team.

Responsibilities

• Collect, validate, and analyze complex chemical, manufacturing, and supply-chain data to identify risks and conclusions.
• Evaluate API and KSM manufacturing processes, sourcing structures, supply-market dynamics, and cost drivers; perform technoeconomic analyses.
• Conduct literature/database reviews to assess processes, routes, suppliers, and technologies.
• Develop clear, evidence-based technical assessments, risk profiles, and recommendations.

Skills

Scientific writing

Analytical skills

Independent work

Team collaboration

Communication skills

Education

Ph.D. in Organic Chemistry

M.Sc. in Organic Chemistry (alternative)

Job description

Who is USP?

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.

Description

Who is USP?

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world’s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.

Brief Job Overview

USP seeks a scientific and technical expert with demonstrated experience in active pharmaceutical ingredients, fine chemicals manufacturing, and associated supply chains, combined with strong technical writing capabilities. This non-laboratory, individual contributor role will apply expertise in pharmaceutical manufacturing and supply chains to evaluate manufacturing processes, assess supply vulnerabilities, analyze technical and market information, and develop practical, evidence-based recommendations for essential medicines. The role will analyze APIs, key starting materials, and excipients; identify manufacturing and supply vulnerabilities; and translate findings into technically sound recommendations, including alternative synthetic routes and advanced manufacturing approaches. The advisor may support multiple donor-funded projects and will be responsible for high-quality technical deliverables completed in accordance with project timelines and applicable quality management procedures.

THIS IS A 2 YEARS FIXED TERM POSTION

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

This role strengthens USP’s ability to identify and address pharmaceutical manufacturing and supply-chain vulnerabilities affecting essential medicines and products. By translating complex chemical, manufacturing, market, and supply-chain information into clear risk assessments and actionable recommendations, this role will support evidence-based decision-making, technically credible interventions, and high-quality delivery across multiple projects.

How will YOU create impact here at USP?

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

This role strengthens USP’s ability to identify and address pharmaceutical manufacturing and supply-chain vulnerabilities affecting essential medicines and products. By translating complex chemical, manufacturing, market, and supply-chain information into clear risk assessments and actionable recommendations, this role will support evidence-based decision-making, technically credible interventions, and high-quality delivery across multiple projects.

The Technical Advisor Has The Following Responsibilities

Technical Assessment and Analysis

• Collect, validate, and analyze complex chemical, manufacturing, and supply-chain data to identify risks, gaps, and technically relevant conclusions.
• Evaluate API and KSM manufacturing processes, sourcing structures, supply-market dynamics, and cost drivers; conduct chemical-process technoeconomic analyses; and identify opportunities to improve supply resilience and manufacturing feasibility
• Conduct structured literature and database reviews to assess manufacturing processes, synthetic routes, suppliers, technologies, and relevant technical evidence.
• Integrate data and scientific judgment to assess manufacturing and supply risks and recommend technically feasible mitigation options, including alternative synthetic routes, process improvements, or advanced manufacturing approaches.

Scientific Writing and Project Delivery

• Develop clear, evidence-based technical assessments, risk profiles, scientific reports, briefing materials, and recommendations tailored to technical and nontechnical audiences.
• Contribute pharmaceutical manufacturing and donor-funded expertise by working closely with chemists and data scientists to align with project goals and meet required implementation timelines.
• Plan and deliver assigned technical workstreams and deliverables in accordance with project scope, quality requirements, timelines, and budget parameter.
• Collaborate with supply-chain specialists, data scientists, project leaders, and other technical experts to integrate scientific findings into project-level risk assessments, recommendations, and implementation approaches
• Prepare SOPs, protocols, reports, and related project documentation.
• Review records and documents.

Who is USP Looking For?

• Ph.D. in Organic Chemistry with minimum 2 years of industrial research experience in API or fine chemical industries; or M.Sc. in Organic Chemistry with minimum 5 years of industrial research experience in API or fine chemical industries.
• Demonstrated scientific and technical writing experience, including the ability to synthesize evidence and develop clear technical assessments, reports, and recommendations.
• Experience conducting independent literature searches, database reviews, and evidence synthesis related to pharmaceutical manufacturing, synthetic routes, suppliers, or technologies.
• Strong analytical, problem-solving, written, and oral communication skills.
• Ability to work independently and collaboratively in a matrixed team environment.

Additional Desired Preferences

• Donor-funded project experience.
• Flow chemistry and PAT.
• Data science/cheminformatics.
• Broader pharmaceutical/fine-chemicals market and supply-chain knowledge.

Benefits

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

Compensation

Base Salary Range: USD $126,250 – $176,509.00 annually.

Target Annual Bonus: % Varies based on level of role.

Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws.

For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

Job Category

Technical Programs

Job Type

Full-Time