Production Supervisor - 2nd Shift and 3rd Shift (m/f/d)

KD Pharma•Miami, FL

6d•$60,000 - $65,000•Onsite

About The Position

The Production Supervisor – 2nd Shift is responsible for leading manufacturing and packaging operations to meet daily production targets while ensuring strict compliance with cGMP, FDA regulations, and internal Standard Operating Procedures (SOPs). This role oversees shift personnel, equipment performance, documentation accuracy, and continuous improvement initiatives, while fostering a safe, positive, and high‑performing work environment.

Requirements

Previous supervisory experience in a manufacturing or packaging environment, preferably FDA‑regulated.
Strong working knowledge of cGMP, SOPs, FDA, and CFR compliance requirements.
Experience with production scheduling, shift management, and workforce planning.
Mechanical aptitude with the ability to identify and resolve equipment issues.
Proficiency in production documentation, batch records, and deviation reporting.
Ability to use basic math for inventory counts, measurements, and quality assessments.
Forklift operation experience or willingness to obtain certification.
Strong leadership, communication, and organizational skills.
Ability to work independently on 3rd shift and make sound decisions under pressure.

Nice To Haves

Leadership and team development
Compliance and quality focus
Continuous improvement mindset
Safety and risk awareness
Clear communication and cross‑functional collaboration

Responsibilities

Supervise and coordinate all production and packaging activities on the 3rd shift to meet output, quality, and ship date objectives.
Solve day‑to‑day production issues and maximize manufacturing efficiency and output.
Ensure all production staff are trained, qualified, and compliant with cGMP, FDA, and SOP requirements.
Plan and manage shift schedules, staffing levels, and overtime to meet production demands.
Conduct daily shift handover meetings with Subject Matter Experts (SMEs) to review performance, issues, and required corrective actions.
Ensure preventive maintenance activities are completed on critical production equipment and coordinate repairs as needed.
Perform routine inspections of equipment and machinery; troubleshoot issues using mechanical knowledge.
Oversee and authorize manufacturing releases, including cleaning approvals, process starts and restarts, documentation review, and batch record completion.
Maintain accurate production logs, sanitation records, quality checks, deviation reports, and other required documentation.
Identify, document, and communicate any deviations related to procedures, processes, or products in accordance with CFR requirements.
Communicate potential delays or late batches promptly and accurately to the Production Manager.
Maintain close collaboration with Quality and Regulatory teams to ensure compliance and issue resolution.
Conduct annual performance reviews and provide ongoing coaching and training to assigned employees.
Promote and enforce safety policies, food safety practices, and a safe working environment.
Support Lean Manufacturing, Manufacturing Excellence, and continuous improvement initiatives across processes, people, equipment, and procedures.