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Production Manager

Location : Valley Cottage NY US 10989
Job Type : Direct
Reference Code : 19452-MK1
Compensation : 85000.00 - 95000.00 USD/YEAR
Hours : Full Time
Required Years of Experience : 5
Required Education : BS Mechanical or Manufacturing Engineering
Travel : No
Relocation : No
Job Industry : Pharmaceutical

Job Description :

  • Permanent position for a Production Manager within the pharmaceutical industry responsible for the management and coordination of assembly operations ensuring production meets output and quality goals while remaining in budget in a cGMP environment.

  • The Production Manager will establish shifts and allocate resources to efficiently maintain assembly operations on schedule.

  • Responsible for the training of assembly operations employees and the discipline and morale of the staff.

  • Create and maintain documentation to ensure proper execution of production processes and adherence to cGMP regulations.

  • Develop production plan by coordinating requirements with sales, engineering, procurement and logistics department.

  • Complete production plan by establishing priorities, scheduling activities and employees, monitoring progress, and resolving problems.

  • Provide manufacturing decision-making information by estimating future requirements on labor and machines.

  • Prepare reports by collecting, analyzing and summarizing information and trends.

  • Ensure that personnel adhere to safety rules and regulations (OSHA, etc.).

  • Regulate or shut down equipment during emergency situations.

  • Participate in product and equipment investigations, report and investigate non- conformities.

Required Qualifications :

  • BS Mechanical or Manufacturing Engineering or AAS with equivalent experience.

  • Minimum 5 years experience with pharmaceutical or biomedical manufacturing operations.

  • Experience with management and leadership of direct labor personnel within pharmaceutical or biomedical manufacturing.

  • Experience establishing production shifts to meet output and quality goals while maintaining budgets.

  • Experience creating and maintaining documentation to adhere to cGMP regulations.

Contact: Monique Kleiman

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