Manufacturing Planning Supervisor
Listed on 2026-07-01
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Manufacturing / Production
Production Manager, Manufacturing Engineer, Quality Engineering
Manufacturing Planning Supervisor
Our client, a growing Cell Therapy company, is looking for a Manufacturing Planning Supervisor. The job responsibilities are as follows:
Production and Warehouse OversightManage and oversee both production and warehouse activities to ensure seamless operations.
Manufacturing SchedulingDevelop and maintain manufacturing schedules to optimize efficiency and meet production targets.
Team SupervisionLead and supervise the manufacturing team, providing guidance and fostering a collaborative work environment.
Quality Assurance and ComplianceEnsure manufacturing processes adhere to high-quality standards and comply with ISO 13485 and FDA regulatory requirements.
Problem Diagnosis and ImprovementIdentify and diagnose issues in the production line, offering recommendations and implementing training programs for continuous improvement.
Process OptimizationDevelop and implement process improvements to maximize production efficiency, utilizing equipment and materials effectively.
Inventory Management and PurchasingSupervise inventory levels, oversee the purchasing of raw materials and equipment, and negotiate favorable terms with suppliers.
Documentation and Operation InstructionsDevelop operation instructions and equipment specifications for production activities.
Training and GuidanceProvide training and guidance to team members to achieve production and warehouse goals.
Best Practices DevelopmentImplement best practices to enhance production capacity, quality, and reliability.
Equipment/Process ValidationParticipate in equipment and process validation activities to ensure compliance with quality standards.
Safety ProceduresEstablish and enforce safety procedures for employees within the manufacturing environment.
Skills Required:
Educational BackgroundDegree in Engineering (Master's degree preferred).
Regulatory KnowledgeKnowledgeable about ISO 13485 and/or cGMP.
ExperienceOver 5 years of experience in a medical devices or pharmaceutical environment.
Analytical SkillsSuperb analytical, problem-solving, and critical thinking skills.
Software ProficiencyProficient in MS Office.
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