This is a Job Description for a Sr Manufacturing Supervisor -- 2^nd^ Shift in Cleveland, Mississippi

Summary: Supervise daily activities in the production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with good current manufacturing practices (cGMPs), SOPs, environmental health and safety (EHS) guidelines and any other regulations that may apply. Supervise and ensure efficiency and effectiveness in various areas. Ensure operational efficiency, troubleshoot and investigate as necessary. Perform all duties with a focus on optimizing safety, quality, service and cost. May supervise more than one department.

Duties & Responsibilities: Communicates guidance, support, direction and leadership through effective interactions with all personnel during daily operations. Supervises the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities. Identify/prioritize/provide resources as appropriate. Interviews, hires, coaches, motivates, develops, recognizes and manages performance of direct reports. Provides regular feedback to all direct reports. Assist in setting performance objectives and development plans and monitor progress. Reviews, approves, and runs documentation for batch and system records. Assists in release of product for distribution. Assists in meeting product release time goals. Identifies, initiates and facilitates continuous improvements, lean manufacturing activities and initiatives, such as 5S, visual management, kaizens. This role may also be responsible for identifying and implementing VIPs. Ensures resources and raw materials are used in the most efficient and productive manner possible. Develops training content and facilitates and verify appropriate training for employees in the area. Ensures compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required. Submits and/or maintains and distributes reports related to attendance, labor, efficiency, safety, scrap and others as needed. Performs/leads technical reviews, investigations and process improvement projects. Provides manufacturing input into integration and validation of new equipment and processes. Resolves technical, material and cGMP problems that may impact project deadlines. Provides guidance and troubleshooting assistance as needed during a deviation in the process. May represent the company during FDA inspections or provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs. May monitor capital expenditure and assist in developing budgets.

 Requirements

and Qualifications[]{#Hlk142289191}[]{#Hlk142304825}

: Bachelor's degree preferred; minimum associate's degree with technical subject area required. And/or 3 years or more of manufacturing experience and 1 year or more of supervisory experience. Proven track record of interpersonal and leadership skills with ability to interface well with other departments and lead effectively and efficiently in a team environment. In-depth process knowledge of related manufacturing equipment and processes. Ability to manage multiple priorities in a manufacturing plant setting. Ability to analyze and interpret scientific and statistical data. Strong professional writing skills and ability to prepare technical reports. Ability to clearly articulate information during regulatory/client inspections.

Equal

Opportunity/Affirmative Action Employer.