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MANUFACTURING PLANNING SUPERVISOR
Jersey City, NJ

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Our client, a growing Cell Therapy company, is looking for a Manufacturing Planning Supervisor.

The job responsibilities are as follows:

 

     1. Production and Warehouse Oversight:

    • Manage and oversee both production and warehouse activities to ensure seamless operations.
  1. Manufacturing Scheduling:

    • Develop and maintain manufacturing schedules to optimize efficiency and meet production targets.
  2. Team Supervision:

    • Lead and supervise the manufacturing team, providing guidance and fostering a collaborative work environment.
  3. Quality Assurance and Compliance:

    • Ensure manufacturing processes adhere to high-quality standards and comply with ISO 13485 and FDA regulatory requirements.
  4. Problem Diagnosis and Improvement:

    • Identify and diagnose issues in the production line, offering recommendations and implementing training programs for continuous improvement.
  5. Process Optimization:

    • Develop and implement process improvements to maximize production efficiency, utilizing equipment and materials effectively.
  6. Inventory Management and Purchasing:

    • Supervise inventory levels, oversee the purchasing of raw materials and equipment, and negotiate favorable terms with suppliers.
  7. Documentation and Operation Instructions:

    • Develop operation instructions and equipment specifications for production activities.
  8. Training and Guidance:

    • Provide training and guidance to team members to achieve production and warehouse goals.
  9. Best Practices Development:

    • Implement best practices to enhance production capacity, quality, and reliability.
  10. Equipment/Process Validation:

    • Participate in equipment and process validation activities to ensure compliance with quality standards.
  11. Safety Procedures:

    • Establish and enforce safety procedures for employees within the manufacturing environment. 

 

Skills Required:

  • Educational Background:

    • Degree in Engineering (Master’s degree preferred).
  • Regulatory Knowledge:

    • Knowledgeable about ISO 13485 and/or cGMP.
  • Experience:

    • Over 5 years of experience in a medical devices or pharmaceutical environment.
  • Analytical Skills:

    • Superb analytical, problem-solving, and critical thinking skills.
  • Software Proficiency:

    • Proficient in MS Office.


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