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Manufacturing Supervisor (Aseptic Filling)

Pharma Universe

N/A


Job Details

Full-time


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Full Job Description

Following the acquisition of a brand-new site in Kansas City, the newly created role of the Manufacturing Supervisor which will be critical in overseeing and optimizing department-specific operations while ensuring quality, safety, and efficiency. If you’re a proven leader with expertise in cGMP regulations and a background in manufacturing within regulated environments, we invite you to apply and join our collaborative team.

Position: Manufacturing Supervisor (Aseptic Filling)

Shift: 3rd shift (10pm-6am)

Location: Kansas City, KS

Responsibilities:

  • Lead daily manufacturing operations, ensuring efficient use of equipment and materials to meet a rapidly expanding production schedule under cGMP guidelines.
  • 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.
  • Ensure operations are efficient and organized.
  • Report non-conforming events immediately and work through the required resolution.
  • Promote a collaborative work environment and find and implement process improvements.
  • Monitor production metrics using databases and spreadsheets, ensuring accurate reporting and compliance with documentation standards.
  • Lead the dedicated 3rd shift operations team

Experience/Qualifications:

  • Associate degree in related discipline or technical certificate preferred, or minimum 3 years related lead/supervisory or lead role experience.
  • 5 years manufacturing experience in pharmaceutical, chemical, food, or other highly regulated environment.
  • Thoroughly understand cGMP regulations and requirements, translate operational details, and communicate with work staff.
  • Prior experience in aseptic manufacturing operations is a must.
  • Hands-on experience with manual visual inspection of PFS and vials.

 

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