Demo

Drug Product Manufacturing Supervisor

Pharma Universe
Chicago, IL Full Time
POSTED ON 1/21/2025
AVAILABLE BEFORE 7/19/2025
We are seeking 2x Drug Product Manufacturing Supervisor to lead aseptic manufacturing operations at the company's Chicago facility. This role is critical in ensuring the production of high-quality products that meet all regulatory requirements, driving the company's ambitious growth plans.

Key Responsibilities:

  • Lead daily manufacturing operations, ensuring efficient use of equipment and materials to meet a rapidly expanding production schedule under cGMP guidelines
  • Mentor and coach team members, conducting performance reviews, and ensuring the development of staff to meet the demands of increased output
  • Ensure compliance with safety and regulatory standards, adhering to company policies, environmental, health, and safety (EHS) regulations, and cGMP requirements
  • Oversee training of personnel on processes, equipment, and Standard Operating Procedures (SOPs), scaling operations effectively as production ramps up
  • Develop and maintain packaging schedules, participate in budget planning, and ensure alignment with departmental goals as output increases
  • Participate in qualification, validation activities, and CAPA investigations to ensure process improvements are implemented efficiently and support scale-up efforts
  • Collaborate across departments to ensure smooth workflow, sharing best practices and applying lean manufacturing principles to maximize output
  • Monitor production metrics using databases and spreadsheets, ensuring accurate reporting and compliance with documentation standards
  • Investigate and resolve production issues, implementing process improvements to support the company's ambitious growth plans


Requirements:

  • Bachelor's degree in engineering, life sciences, or a related field. A Master's degree is an asset
  • Prior experience in aseptic manufacturing operations is a must
  • Hands-on experience with manual visual inspection of PFS and vials
  • Experience in finished product packaging and serialization is highly preferred
  • Strong leadership and communication skills, with the ability to guide teams through rapid operational growth
  • Problem-solving expertise, with a focus on maintaining high standards of quality and efficiency
  • Proficiency in technical writing, including the ability to author SOPs and manage deviations
  • In-depth knowledge of cGMP and FDA regulatory requirements

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