Supervisor Manufacturing

The Manufacturing Supervisor is responsible for the oversight of daily GMP manufacturing operations, ensuring production activities are executed in a safe, compliant, and efficient manner. This role provides direct supervision of manufacturing personnel, ensures strict adherence to cGMP requirements, maintains real-time documentation integrity, and serves as the primary operational escalation point for the assigned shift.Schedule:3rd shift (4PM to 4AM), every Wed., Thurs., & every other weekendProduction Execution & Shift OversightAbility to understand and operate process equipment.Ensures timely and accurate execution of manufacturing instructions.Monitor ongoing operations and address routine issues in real time.Serve as the primary point of contact for the shift activities.Communicate production status, issues, and lead the shift change meetings.Ensures the proper systems and resources are in place to meet production schedules on time and that product is manufactured to specification and in accordance with SOP's and cGMP's, company policies and safety procedures.Monitors and controls production schedules and activities to ensure meeting of departmental performance objectives and budgets.Supervises, coordinates, and controls the day-to-day production and operating activities to ensure optimum utilization of personnel, materials and equipment.Ensures adequate resources are available to manufacture product (equipment, supplies, and labor).Develops information and compiles reports concerning scheduling, production goals, equipment and maintenance problems and other studies and/or reports as needed.Assists in developing production schedules; confers with department managers and Department Head to coordinate the scheduling of operations to achieve required deadlines.Quality, Documentation & cGMP ComplianceReview batch records, logbooks, and documentation in real time for completeness and accuracy.Enforce proper documentation practices (ALCOA+ principles).Promote a right first-time mentality to reduce errors within the team’s control.Escalate deviations, non-conformances, and safety concerns in a timely manner, as needed.Participate in investigations related to deviations, incidents, or out of specification results including taking appropriate immediate actions and escalation, as needed.Maintains compliance with company policies, SOP's, cGMP's, safety standards and housekeeping practices.Support and participate in internal and external audits and regulatory inspections and audit readiness activities.Safety & Environmental CompliancePromote a strong culture of safety and quality on the floor.Ensure compliance with and proper use of PPE and adherence to manufacturing gowning procedures.Escalate safety concerns and incidents in a timely manner as needed.People Leadership & Workforce ManagementDirectly supervise operators and ensure staff are properly trained and qualified to execute assigned tasks.Maintain shift coverage, including scheduling and attendance tracking. Create the finite schedule for the assigned team.Supervises hourly operators in proper operating techniques and procedures.- Coaches, trains, develops, disciplines and recognizes employees, including conducting performance reviews.Develops department employees through establishing objectives, communication of rules and policies while building employee morale and motivation.Troubleshooting, Investigations & Continuous ImprovementAssist with troubleshooting equipment and process issues.Investigates and resolves problems, identifies root cause, and clearly communicates to senior management.Identify opportunities for process improvement and communicate them to management.Support or lead actions to implement process improvements.Advises department management on matters relating to daily operations and makes recommendations for process improvements.Cross Functional Collaboration & ReportingCollaborate with Quality, Maintenance, Warehouse, and other teams as necessary.Participate in multi-functional teams as needed.Interacts without outside vendors and senior management as needed.Process monitoring, including manipulation of databases, documents and/or spreadsheets to support business reporting requirements.Job Requirements and Qualifications:Associate degree required; Bachelor’s degree or above preferred.Experience in lieu of education may be considered.3+ years required cGMP Manufacturing and 1+ years leadership preferred.You should be proficient in:Good Manufacturing Practices (GMP)Production SchedulesSOP'sPPE #J-18808-Ljbffr