Manufacturing Operations Leader

6 days ago


Somerville, New Jersey, United States AbbVie Full time
Job Summary

The Manufacturing Supervisor role offers a dynamic opportunity to lead and train a team of operating personnel in the production of clinical or commercial products. By ensuring accurate documentation and adherence to cGMP standards, you will play a vital role in maintaining product quality.

Key Responsibilities
  • Develops Weekly Goals and Schedules: Develops and implements weekly goals and schedules for staff, prioritizing tasks and ensuring efficient use of resources.
  • Reviews Production Schedule and Priorities: Reviews the weekly production schedule and priorities to determine unit assignments and critical actions, ensuring alignment with business objectives.
  • Provides On-the-Floor Training: Provides on-the-job training to support formalized technical and GMP training, ensuring operators have the necessary skills to perform their duties effectively.
  • Monitors Operator Training Files: Monitors operator training files and works with the compliance specialist to ensure files are up-to-date and compliant with regulatory requirements.
  • Resolves Exceptions and Issues: Works with QA and subject matter experts to resolve exceptions and issues related to production, ensuring timely resolution and minimal disruption to operations.
  • Collaborates with Cross-Functional Teams: Collaborates with cross-functional teams, including technology transfer, to incorporate new processes and improve manufacturing operations.
  • Ensures Compliance and Quality: Ensures compliance with cGMP standards and quality systems, maintaining a culture of excellence and continuous improvement.
  • Leads and Develops Team Members: Leads and develops team members, providing guidance, coaching, and feedback to ensure their growth and success.
Requirements
  • Education and Experience: Bachelor's degree or equivalent, with 8+ years of experience in all aspects of GMP manufacturing/packaging processes.
  • Technical Skills: Computer proficiency, scheduling experience, and good writing skills are required. Working knowledge of safety, quality systems, and cGMP manufacturing/packaging is essential.
  • Leadership and Management Experience: At least 5 years of leadership/management experience, including managing production personnel.


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