Supervisor Heparin Operations - Sioux City, IA

Our Supervisor Heparin Operations is responsible for leading daily operations within our cGMP compliant manufacturing facility. This position is responsible for supervising production personnel, ensuring compliance with cGMP standards, and driving safe, efficient, and on-time manufacturing operations.

The ideal candidate is a hands-on leader with manufacturing experience, strong problem-solving skills, and the ability to motivate teams while maintaining a focus on quality, safety, and productivity. Join our Mobren Transport team located in Sioux City, IA. Apply today!

Job Responsibilities:

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. Supervises hourly operators in proper operating techniques and procedures. Coaches, trains, develops, disciplines and recognizes employees, including performance reviews. Develops department employees through establishing objectives, communication of rules and policies while building employee morale and motivation. Assists in developing production schedules; confers with department manager to coordinate the scheduling of operations to achieve required deadlines. Monitors and controls production schedules and activities to ensure the meeting departmental performance objectives. Supervises, coordinates and controls the 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). Maintains compliance with company policies, SOP's, cGMP's, safety standards and housekeeping practices. Advises department management on matters relating to daily operations and makes recommendations for process improvements. Investigates and resolves problems, identifies root cause, and clearly communicates to senior management. Process monitoring, including manipulation of databases, documents and/or spreadsheets to support business reporting requirements. Interacts without outside vendors as needed.

Job Requirements:

• Associate's degree.
• 2 years of manufacturing or production leadership experience.
• Experience working in a cGMP-regulated manufacturing environment.
• Previous supervisory, or team lead experience.
• Ability to coordinate labor, materials, equipment, and resources to support production needs.
• Knowledge of SOPs, safety procedures, quality systems, and regulatory compliance.
• Ability to manage production schedules and ensure production goals are achieved.
• Experience using spreadsheets, databases, and production reporting tools.
• Strong communication, organizational, and interpersonal skills.
• Experience coaching, training, and developing production employees.
• Ability to work in a fast-paced manufacturing environment and manage multiple priorities.
• Ability to lift up to 50-75 lbs. occasionally and perform physical production-floor activities.

Preferred:

• Bachelor's degree.
• 5 years of manufacturing or production leadership experience.
• Ability to work extended hours as needed to meet production demands.
• Experience working directly with vendors, suppliers, or external partners.
• Ability to investigate operational issues and communicate findings to senior management.
• Experience monitoring production metrics, budgets, and operational performance.
• Familiarity with continuous improvement initiatives and process optimization.
• Experience conducting performance reviews and managing employee performance.
• Previous experience using QMS, CMMS, WMS, or other computerized warehouse or inventory management systems.