Your Tasks:
* Develop and maintain detailed production schedules for biopharmaceutical manufacturing processes
* Coordinate with cross-functional teams including production, quality assurance, supply chain, maintenance, calibration, and engineering to ensure alignment and efficient workflow
* Monitor production progress and adjust schedules as necessary to address changes in priorities, equipment availability, and other factors
* Analyze production data to identify bottlenecks, delays, and opportunities for process improvements
* Ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements
* Communicate schedule changes and production status updates to relevant stakeholders
* Participate in production meetings and provide insights on scheduling impacts
* Maintain accurate records of production schedules, adjustments, and performance metrics
Your Qualifications:
* Bachelor’s degree in Industrial Engineering, Manufacturing, Biotechnology, or a related field
* Solid experience in production scheduling, preferably in a biopharmaceutical or pharmaceutical manufacturing environment
* Strong understanding of GMP and regulatory requirements in biopharma manufacturing
* Proficiency in production scheduling software and tools (e.g., SAP, Oracle, MS Project, Smartsheet)
* Excellent organizational, analytical, and problem-solving skills
* Strong communication and interpersonal skills
* Ability to work in a fast-paced, dynamic environment and manage multiple priorities
Seniority level
Associate
Employment type
Temporary
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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