2nd Shift Process Supervisor: Lean Manufacturing Leader

RXinsider LTD.; Cherry Hill Township (NJ); On-site; USD 57,000 - 95,000; Full time

Job summary

Hikma Pharmaceuticals USA Inc. in Cherry Hill, NJ, is seeking a Process Supervisor for 2nd shift (3:00 PM–11:30 PM). You will manage shift operations in manufacturing, drive cost reductions, uphold safety and quality, and guide staffing decisions to meet budgets and production goals.

The role requires 5–7 years of manufacturing experience, a technical B.S. or equivalent, and strong knowledge of Lean and GMP practices to ensure regulatory compliance and continuous improvement.

Qualifications

• B.S. or equivalent in a technical field or 10 years of pharma injectables manufacturing as alternative.
• 5-7 years experience in manufacturing processes.
• Ability to manage department activities through subordinates with cost and staffing oversight.
• Ability to interpret statistical data and financial reports and resolve technical issues.
• Knowledge of Lean, GMP, FDA guidelines, and process validation.

Responsibilities

• Meet production requirements and deliver quality products on time and cost-efficiently.
• Identify resources to help meet operating plan and budget commitments.
• Supervise daily manufacturing operations across one or more departments.
• Provide training and implement control systems to reduce product discrepancies.
• Make staffing decisions and manage disciplinary issues.
• Drive operational excellence and Lean manufacturing culture.

Skills

Manufacturing experience

Lean manufacturing

GMP knowledge

Statistical data interpretation

Budgeting understanding

Education

B.S. or equivalent

Job description

Hikma Pharmaceuticals USA Inc. in Cherry Hill, NJ, is seeking a Process Supervisor for 2nd shift (3:00 PM–11:30 PM). You will manage shift operations in manufacturing, drive cost reductions, uphold safety and quality, and guide staffing decisions to meet budgets and production goals.

The role requires 5–7 years of manufacturing experience, a technical B.S. or equivalent, and strong knowledge of Lean and GMP practices to ensure regulatory compliance and continuous improvement.