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UPSTREAM / DOWNSTREAM MANUFACTURING SUPERVISOR

Pharma Universe
Chicago, IL Full Time
POSTED ON 3/7/2025
AVAILABLE BEFORE 6/4/2025

To support this next phase, we are recruiting for a Drug Substance Supervisor who will play a critical role in managing the production activities for Biologics Manufacturing for the 3rd shift operation. This includes supervising cell culture fermentation, protein purification, and aseptic processing to produce high-quality drug substances.

Responsibilities :

  • A working supervisor position is shift lead.
  • Participate in all drug substance related manufacturing process. Perform (Where needed) and review the process to ensure compliance with the requirements listed in respective batch record.
  • Provides daily supervision on the floor to personnel in the efficient use of equipment and materials to produce quality products under cGMP in accordance with the production plan.
  • Provides coaching, counseling, development, discipline and recognition of direct staff, including performing annual performance reviews.
  • Responsible for maintaining alignment with department direction, goals and objectives.
  • Promotes the use of safe work practices during all production and ensures all external and company policies and EHS standards are met daily.
  • Responsible for training personnel on equipment, processes and Standard Operating Procedures (SOPs).
  • Trains and develops personnel, develops and maintains packaging schedules, and manages within the department budget.
  • Ensures that projects are completed on schedule per established procedures.
  • Participate in execution of qualification and validation activities.
  • Participate in process related investigation(s) and implement CAPA derived from investigation outcome in timely manner.
  • Author and reviews SOPs and other documents to ensure integration of cGMPs and improve process efficiency.
  • Works collaboratively to ensure flow of product, sharing of best practices and lean behaviors.
  • Performs process monitoring, including use of databases, documents and / or spreadsheets to support business reporting requirements.
  • Performs ongoing operational tasks of organization unit, actively assists, or provides direction to subordinates as required.
  • Responsible for final review of completed documentation per compliance standards and establish timelines.
  • Investigates and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior management.
  • Participation and / or leadership role in multi-functional project teams as necessary.
  • Other tasks as requested by management.

Experience / Qualifications :

  • Bachelor's degree, in engineering, pharmaceutical, related life science and at least 5 years of experience
  • Master's degree, in engineering, pharmaceutical, related life science and at least 2 years of experience
  • Upstream and Downstream manufacturing experience
  • Prior Drug Substance Manufacturing experience
  • Prior aseptic process execution and supervisory experience is strongly preferred.
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