Manufacturing Supervisor (Fill/Finish)

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 (Fill/Finish)

Shift: 2nd Shift (2pm-10pm)

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 2nd 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.