Expires soon Novartis

Clinical Production Planning & Schedule Control Associate

  • Morris Plains (Morris County)
  • Bachelor's Degree
  • Design / Civil engineering / Industrial engineering

Job description

Job Description

Local candidates only. No relocation available.

PURPOSE
Working under limited supervision, the Clinical Production Planning and Schedule Control Associate is responsible for developing and managing the execution of the supply plan based on agreed upon safety stock levels while optimizing clinical production operations.

RESPONSIBILITIES
• Execution of Clinical Production Plan. • Ensures applicable coverage of materials to meet manufacturing and packing plans. • Ensure transparency and priorities of orders. • Establish optimum cycle to maximize flexibility, while minimizing WIP. • Participation on monthly Demand Management team.
• Determine and inform production priorities and overtime requirements.
• Supply Chain Principles – understanding of Materials Management principles such as (but not limited to) MPS, MRP, CRP, DRP, SFC, purchasing, distribution, import/export, transportation, etc. • Pharmaceutical Production – knowledge of pharmaceutical operations and industry practices. Knowledge of Good Manufacturing Practices. (cGMPs). • Working knowledge of SAP and ability to learn cell chain software systems

EEO Statement

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

Desired profile

Minimum requirements

EDUCATION: •Bachelor of Science in Logistics, Business, Industrial Engineering or Operations Research preferred. • APICS certification strongly desired.

EXPERIENCE: 2-4 years planning experience in a pharmaceutical operations environment. • Experience working in a GMP environment. • Knowledge of pharmaceutical principles and supply chain practices and software systems.

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