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Supervisor Manufacturing

Job in Clearwater, Pinellas County, Florida, 34623, USA
Listing for: Bend Bioscience
Full Time position
Listed on 2025-12-02
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Operations / Plant Manager
Job Description & How to Apply Below

At Bend Bioscience, our core values shape how we work, lead, and grow together.

We are a High Science, High Service, people-centered company committed to advancing human health. Our team thrives on being authentic, curious, and accountable, while staying flexible, collaborative, and driven by care. We blaze trails by challenging the status quo, pursuing excellence in everything we do, and maintaining relentless focus on delivering real impact.

Whether you are in the lab, on the floor, or behind the scenes, your work at Bend Bioscience will matter. You will join a team that values continuous learning, bold thinking, and doing the right thing—even when it is hard.

Leadership Functions (Responsibilities)
  • Provide daily oversight and direction to the Manufacturing Department, ensuring alignment with company policies and production goals.
  • Coach, develop, and engage team members to build a cohesive, high-performing, and inclusive team culture.
  • Identify, recruit, and retain qualified talent to support departmental success.
  • Set clear performance expectations and foster growth through delegation, feedback, goal setting, and performance management.
  • Communicate organizational updates and departmental priorities through meetings, email, and interpersonal interactions.
Essential Functions (Responsibilities)
  • Supervise daily manufacturing operations, including equipment use, process troubleshooting, and coordination with cross-functional departments.
  • Participate in investigations, equipment qualifications, validation activities, and internal audits to support compliance and continuous improvement.
  • Monitor cleanliness, safety, and organization of manufacturing areas, ensuring adherence to SOPs and safety guidelines.
  • Coordinate scheduling of events such as equipment calibration, maintenance, and cleaning to minimize production impact.
  • Ensure accuracy of batch records prior to Quality Assurance review and maintain documentation related to attendance, labor, efficiency, and safety.
  • Collaborate with Material Services to manage inventory and warehouse-related issues for raw materials and finished products.
  • Monitor handling and documentation of controlled substances during transport and processing.
Minimum Required
  • High school diploma or equivalent.
  • Preferred:
    Bachelors.
Experience
  • Required:

    6 plus years in solid oral dose pharmaceutical manufacturing.
  • Preferred People Management: 1 plus years.
  • Will Accept:
    With Bachelors, 4 plus years in solid oral dose pharmaceutical manufacturing.
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