P

Phlow

Domestic API and FDP CDMO services

Senior Scientist - Analytical Chemistry

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeRichmond, VA, USA

About the Job

Requirements

  • Independently conduct analytical method development, validation, and project support.
  • Identify technical challenges during analytical method development and perform analytical method troubleshooting.
  • Manage contract manufacturing organization and contract research organization analytical project resources, such as contractors and contract laboratories, as needed.
  • Manage the technical direction of analytical projects; identify key deliverables and next steps and communicate them to the team.
  • Produce, review, analyze, and interpret data from a variety of sources; provide accurate summaries and recommendations to stakeholders with scientific rigor.
  • Author and review technical reports, regulatory submissions, standard operating procedures, validation protocols, and other current Good Manufacturing Practice documents.
  • Perform assigned analytical tasks with minimum supervision in support of product development and clinical trial material.
  • Perform activities within assigned timelines and in compliance with current Good Manufacturing Practice, regulatory requirements, and company practices and procedures.
  • Design and conduct studies in accordance with company and regulatory standards to facilitate new product development.
  • Manage day-to-day laboratory activities for analytical equipment, including sourcing consumables, troubleshooting, maintaining equipment, and coordinating calibrations with vendors.
  • Have an advanced degree in chemistry, pharmaceutics, or a related field.
  • Have 1–3 years of experience in analytical method development, validation, and API and/or drug product development activities regulated by the FDA.
  • Have working knowledge of standard Office tools, including Microsoft Office, Microsoft Project, Excel, Visio, and SharePoint.
  • Have functional expertise in analytical chemistry, compound purification, and spectral analysis and interpretation.
  • Have experience with common analytical techniques, including HPLC, LC/MS, GC, GC/MS, Karl Fischer, loss on drying, DSC, TGA, NMR, UV, and LC-MS.
  • Have strong interpersonal skills.

Responsibilities

  • Provide analytical chemistry support to Phlow.
  • Support Phlow’s contract development and manufacturing services, including execution of internal API development and commercial projects.
  • Work in accordance with safety, integrity, transparency, and ethics standards.
  • Ensure assigned activities meet timelines and applicable regulatory and company requirements.
  • Conduct studies to facilitate new product development.
  • Manage analytical laboratory equipment and its associated consumables, troubleshooting, maintenance, and calibration.

Desired Qualifications

  • Ph.D. with a minimum of 2 years of experience, M.S. with a minimum of 5 years of experience, or B.S. degree with a minimum of 10 years of experience in Analytical Chemistry, Pharmaceutical Sciences, or a related scientific field.
  • Knowledge of International Council for Harmonisation requirements and current Good Manufacturing Practice requirements.
  • Experience working for a contract organization, such as a contract research organization, contract manufacturing organization, or contract development and manufacturing organization.
  • Experience with technical and operational risk assessments, such as process robustness, mutagenic impurities, and nitrosamines.
  • Experience with the development and implementation of Process Analytical Technology.
  • Experience with Design of Experiments.

About the Company

Phlow

Domestic API and FDP CDMO services

Phlow operates as a US-based CDMO that develops and manufactures Active Pharmaceutical Ingredients (APIs) and Finished Drug Products (FDPs) in the United States. Its services cover research, development, and production of APIs and key starting materials to help customers design and scale drug substances, with a focus on domestic sourcing. The company differentiates itself by prioritizing a reliable US supply chain through government contracts and partnerships with healthcare providers and drugmakers, reducing dependence on foreign manufacturing. Its goal is to build a resilient, domestically produced supply of essential medicines and improve access and reliability for critical medications.

Company size
51-200
Company stage
Series C
Total funding
$122.2M
Headquarters
Richmond, VA
Founded
2020

Recently Posted Jobs

Explore more opportunities at Phlow

See more jobs