Operations Manager

7 days ago


Saddle Brook, New Jersey, United States Lynkx Staffing LLC Full time
Job Overview

Lynkx Staffing LLC is a leading staffing agency specializing in the Biotechnology, Pharmaceutical, and Medical Devices industries in New Jersey. As an Associate Director of Manufacturing Operations, you will play a crucial role in optimizing operations resources to meet customer demand.

Responsibilities
  • Develop and implement strategies for efficient utilization of Operations resources.
  • Oversee site Operations scheduling and training capacities, ensuring timely completion of tasks and projects.
  • Manage all Operations scheduling, training, and compliance activities, maintaining high standards of quality and regulatory compliance.
  • Create and enforce Operator training schedules to ensure production schedules can be carried out smoothly.
  • Maintain accurate and fair personnel schedules, ensuring all Associates are assigned tasks accordingly.
  • Support special long-term projects identified by the PPU Head, driving continuous improvement and process enhancements.
  • Develop and maintain Operations-based Key Performance Indicators (KPIs), ensuring data-driven decision-making.
  • Ensure department staff comply with corporate and site-specific HR policies, safety, and business practices.
  • Approve job-specific curriculum for training and professional development of department staff.
  • Streamline the batch record review process, improving efficiency and reducing errors.
  • Understand profit and loss for the PPU's, including related documentation and its impact on Operations.
  • Drive continuous improvement across the organization, fostering a culture of excellence.
  • Liaise with support groups, including Supply Chain, Training, Quality Systems, Quality Assurance, Quality Control, and others.
Requirements
  • Bachelor's degree in Biology, Biotechnology, Bioengineering, Chemical Engineering, or a related field.
  • 5-10 years of experience in a cGMP environment, with expertise in aseptic processing, mammalian cell culture, monoclonal antibody, cell processing, cryopreservation, or similar areas.
  • 5-10 years of leadership experience or an equivalent combination of experience and skills.
  • Deep understanding of cGMP and cGLP principles.
  • Working knowledge of financial operations and budget development.
  • Relevant IT skills, including Microsoft Office and corporate scheduling systems.
Salary and Benefits

We offer a competitive salary range of $120,000 - $160,000 per year, depending on experience, plus comprehensive benefits, including health insurance, retirement plans, and paid time off.



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