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Phlow

Domestic API and FDP CDMO services

Supervisor - Chemical Processes

Machine & Process OperationConfirmed live in the last 24 hours
Full-timePetersburg, VA, USAIn-person

About the Job

Requirements

  • Ability to work in a fast-paced environment.
  • Must be able to work in a chemical manufacturing plant at both large and small scale.
  • Working knowledge of the Microsoft Office suite and standard office equipment.
  • Working knowledge of Lean Manufacturing concepts.
  • Experience with Root Cause Analysis tools.
  • Experience with potent compounds.
  • Experience with change management.
  • Knowledge of chemical manufacturing and plant support systems.
  • Understanding and working knowledge of current Good Manufacturing Practices.
  • Ability to analyze, prioritize, and manage multiple tasks.
  • Mechanical knowledge of production equipment.
  • Bachelor's degree in a Science or Engineering discipline.
  • Three to five years of previous experience in development, manufacturing, or analytical chemistry.
  • Ability to lift objects weighing up to 55 pounds routinely.
  • Ability to frequently reach, bend, twist, turn, and climb, and to walk, stand, or climb stairs or crossovers for extended periods, including working at heights above 4 feet.
  • Ability to work in varying positions for prolonged durations and safely climb stairs and ladders.
  • Ability to work in indoor factory and outdoor environments with varying temperatures, chemical exposure, and high noise levels.
  • Willingness and ability to wear required personal protective equipment, including respirators, gloves, safety glasses, and protective clothing.
  • Manual dexterity and physical stamina to operate tools and machinery and handle chemical processing and equipment.
  • Ability to follow multi-step instructions of up to three steps accurately.
  • Near and far visual acuity to operate equipment, read gauges, and monitor processes.
  • Ability to work nights, weekends, holidays, and rotating shifts as operational needs dictate.

Responsibilities

  • Supervise and coordinate front-line pharmaceutical manufacturing operations, ensuring compliance with Good Manufacturing Practices, company procedures, and safety requirements.
  • Oversee a team performing small- to large-scale pharmaceutical manufacturing using batch and continuous manufacturing processes.
  • Provide technical guidance, assign work, monitor performance, and ensure safe, efficient, and compliant production under changing operating conditions.
  • Submit maintenance work orders and issue safe work permits as needed to maintain building equipment.
  • Supervise and coordinate daily manufacturing operations, including assigning work, monitoring productivity, and ensuring adherence to Good Manufacturing Practice, safety, and operational procedures.
  • Lead and develop manufacturing personnel through coaching, training, performance feedback, and direction during shift operations.
  • Manage operational incidents, including preparing daily status reports, delegating resources, resolving conflicts, and using internal support systems as needed.
  • Use operational data and performance metrics to track trends, identify improvement opportunities, and make data-driven decisions supporting production objectives.
  • Lead and participate in root cause investigations for process deviations, variances, equipment issues, and safety incidents, and ensure corrective and preventive actions are implemented.
  • Conduct daily Tier meetings, communicate key performance indicators, review safety and quality metrics, and facilitate forward-looking production planning.
  • Review and approve manufacturing documentation and ensure timely completion and accuracy of batch records, logbooks, investigations, and related Good Manufacturing Practice records.
  • Coordinate with Quality, Engineering, Maintenance, EHS, Supply Chain, and internal and external support groups to resolve issues and maintain uninterrupted operations.
  • Provide technical oversight and troubleshoot chemical manufacturing processes, escalating issues as appropriate.
  • Serve as the primary shift contact with outside emergency responders and service providers when required.
  • Ensure effective shift-to-shift communication and keep management informed of significant activities, risks, and operational performance.
  • Ensure specified product quantity levels, including raw materials and product specifications, are available.
  • Drive cost savings through improvements and lean implementation.
  • Establish and maintain detailed records.
  • Design and implement work methods and procedures to increase productivity and improve service within the assigned department.
  • Participate in budget preparation while tracking and establishing progress toward organizational goals.
  • Support a 24/7 manufacturing environment, including coverage for 8–12-hour shifts, nights, weekends, holidays, and rotating schedules as needed.

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
$117.2M
Headquarters
Richmond, VA
Founded
2020

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