Pharmaceutical Manufacturing Program Analyst at BryceTech

Washington, District of Columbia, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Mar, 26

Salary

0.0

Posted On

12 Dec, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmaceutical Manufacturing, Supply Chain Analysis, Quality Assurance, Quality Control, Technical Analysis, Project Management, Regulatory Policy, Trade Policy, Communication Skills, MS Office Proficiency, Adobe Acrobat, Operations Management, Stakeholder Engagement, Research, Documentation, Compliance

Industry

Engineering Services

Description

Company Description BryceTech is a trusted leader in complex technology domains, delivering data-driven solutions in aerospace, biosecurity, and defense. We specialize in systems engineering, advanced analytics, and R&D program and operations support. Our clients – including NASA, DoD, HHS, DHS, and other civil and national security agencies – rely on us to drive mission success and accelerate innovation. BryceTech has been recognized in the Washington Technology Fast 50 ranking of top high-growth small businesses for four consecutive years and received a GovCon Contractor of the Year Award in 2023 and 2025, underscoring our strong growth, competitive positioning, and excellence in federal contracting. With a proven track record of winning sought after contracts, scaling high-performance teams, and executing on critical government missions, BryceTech presents a compelling opportunity for strategic partnerships in the GovCon space. Job Description BryceTech is currently looking for a Pharmaceutical Manufacturing Program Analyst. The person in this role will support a high-visibility HHS ASPR client managing over $21B in portfolio value with a variety of needs including support to the project team and domestic supply chain analysis efforts. Specifically, this person will provide analysis on the technical and programmatic progress of ongoing manufacturing scale-up efforts, and the assessment of novel approaches to domestically produced Active Pharmaceutical Ingredients (API’s), key starting materials, and excipients. This is a dynamic position for a person with attention to detail and adaptability to changes in regulatory policy, trade policy, and shifts in the global supply chain for pharmaceutical materials. Work will be performed on a hybrid schedule in Washington D.C. The person in this role will: Advise on innovative approaches for the successful development, manufacture, and distribution of drug product, APIs, excipients, and key starting materials, and/or related products. Identify and propagate QA/QC best practices with our industry partners to improve manufacturing, testing, distribution, and reporting processes. Support Engagement with manufacturers, commercial labs, upstream suppliers, and distributors, to include: Take and compile meeting notes from calls with manufacturers, commercial labs, test manufacturers, upstream suppliers, and distributors. Track communications and check-ins with manufacturers, commercial labs, test manufacturers, upstream suppliers, and distributors. Draft follow-ups for Industry Engagement Team from check-in calls. Provide technical and QA/QC review of materials before distribution and/or storage to ensure clarity and accuracy of collected and shared information. Operations Management: Provide operational and project management support for office/division/branch activities. Provide analysis of technical reports, integrated master schedules, audit findings, and financial status. Prepare and draft and final report(s), including formatting and document QA/QC for submission. Provide analysis, research, and recommendations on all quality standard operating procedures, policy, processes and procedures, and associated regulations, to assure compliance with the Quality Management System. Develop, manage, and maintain liaison relationships with other HHS Offices and Operating Divisions, other U.S. federal agencies, and non-USG partners (e.g., stakeholder organizations, private sector entities, and research and academic institutions, etc.) Qualifications Master’s Degree in biology, chemistry, or supply chain related field of study 15+ years of experience in pharmaceutical product manufacturing. Experience with synthetic chemistry processes and API production are highly preferred PMP certification preferred Excellent verbal and written communications skills Proficiency with all MS Office product and Adobe Acrobat Additional Information BryceTech offers a full range of benefits, including competitive salary, a comprehensive health plan including dental and vision coverage, company-paid life & disability insurance policies, 401(k) plan with company match, and an educational reimbursement program. All your information will be kept confidential according to EEO guidelines.

Responsibilities

The Pharmaceutical Manufacturing Program Analyst will provide analysis on the technical and programmatic progress of manufacturing scale-up efforts and assess novel approaches to domestically produced pharmaceutical materials. They will also support engagement with various stakeholders and provide operational and project management support.