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Manufacturing Planning Supervisor

Job in Passaic, Passaic County, New Jersey, 07055, USA
Listing for: MRINetwork
Full Time position
Listed on 2026-07-01
Job specializations:
  • Manufacturing / Production
    Production Manager, Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below

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 Oversight

Manage and oversee both production and warehouse activities to ensure seamless operations.

Manufacturing Scheduling

Develop and maintain manufacturing schedules to optimize efficiency and meet production targets.

Team Supervision

Lead and supervise the manufacturing team, providing guidance and fostering a collaborative work environment.

Quality Assurance and Compliance

Ensure manufacturing processes adhere to high-quality standards and comply with ISO 13485 and FDA regulatory requirements.

Problem Diagnosis and Improvement

Identify and diagnose issues in the production line, offering recommendations and implementing training programs for continuous improvement.

Process Optimization

Develop and implement process improvements to maximize production efficiency, utilizing equipment and materials effectively.

Inventory Management and Purchasing

Supervise inventory levels, oversee the purchasing of raw materials and equipment, and negotiate favorable terms with suppliers.

Documentation and Operation Instructions

Develop operation instructions and equipment specifications for production activities.

Training and Guidance

Provide training and guidance to team members to achieve production and warehouse goals.

Best Practices Development

Implement best practices to enhance production capacity, quality, and reliability.

Equipment/Process Validation

Participate in equipment and process validation activities to ensure compliance with quality standards.

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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