Manufacturing Operations Manager

2 days ago


Chicago, Illinois, United States Global Life Science Hub Full time
Manufacturing Supervisor (DP) Job Description

Our client, a leading pharmaceutical company, is seeking a skilled Manufacturing Supervisor (DP) to join their dynamic team in Chicago, IL. As a Manufacturing Supervisor (DP), you will play a crucial role as a shift leader in their manufacturing operation, ensuring the production of high-quality products in compliance with regulatory requirements, operational plans, and company policies.

Key Responsibilities:
  • Production Oversight: Supervise and guide production floor personnel to ensure efficient use of equipment and materials for high-quality product outcomes in accordance with cGMP and production plan.
  • Staff Development: Provide coaching, counselling, and development to direct staff, conducting annual performance reviews.
  • Department Alignment: Maintain alignment with department goals and objectives.
  • Compliance and Safety: Promote safe work practices and compliance with policies, environmental, health, and safety standards.
  • Training and Development: Train personnel on equipment, processes, and SOPs.
  • Packaging Scheduling: Develop and manage packaging schedules within budget.
  • Project Management: Ensure timely project completion and participate in qualification and validation activities.
  • Problem-Solving: Investigate and resolve problems, propose process improvements, and foster collaboration.
  • Process Monitoring: Monitor processes, generate reports, and provide operational direction.
  • Documentation: Review documentation for compliance standards and establish timelines.
  • Team Collaboration: Participate in multi-functional project teams and perform additional tasks as required.
Requirements:
  • Education: Bachelor's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 4+ years of experience.
  • Experience: Master's degree in engineering, pharmaceuticals, related life sciences, or equivalent with 2+ years of experience.
  • Preferred Experience: Preferred experience in aseptic processing, manual visual inspection, and finished product packaging with serialization.
  • Skills: Strong communication, leadership, and problem-solving skills.
  • Technical Skills: Proficient in technical writing, MS Office applications, and leading operational teams.
  • Regulatory Knowledge: Familiarity with FDA cGMPs and regulations.
  • Work Environment: Ability to work in office and biotechnology manufacturing environments.
  • Flexibility: Flexibility for different shifts, overtime, and travel.

The Global Life Science Hub is a niche Life Science headhunting firm. We place professionals across Europe and the US for a variety of Biotechnology, Pharmaceutical, and CRO companies ranging from small start-ups to large global organisations.



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