Pharmaceutical Manufacturing Program Analyst
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Job Location:
Washington, AR - USA
Monthly Salary:
Not Disclosed
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
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 (APIs) 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 :
- Masters 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.
Remote Work :
No
Employment Type :
Full-time
Key Skills
- Project / Program Management
- Program Management
- Data Collection
- Military Experience
- Microsoft Powerpoint
- Earned Value Management
- Sharepoint
- Microsoft Project
- Budgeting
- DoD Experience
- Financial Management
- Contracts
About Company
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 strategic advisory support. Our clients – including NASA, DoD, HHS, DHS, ... View more
