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← Iovance Biotherapeutics

Master Scheduler

Iovance Biotherapeutics
Location
Philadelphia, PA
Posted
1 month ago
Department
0086-ICTC SUPPLY CHAIN
What they actually want (must-haves)
  • 1-2 years scheduling experience in a high-volume cGMP production or manufacturing environment
  • Bachelor’s Degree in Supply Chain, Business Management, or Engineering
  • Working knowledge of MRP/ERP systems
  • Proficient in MS Word, Excel, Outlook, PowerPoint
  • Ability to collaborate across disciplines
  • Strong interpersonal and team-building skills
Nice to have
  • 3-5 years scheduling experience in a high-volume cGMP production or manufacturing environment
  • Experience using SmartSheet
  • Experience using Claude or other AI tools
  • Facilitated collaborative discussions/meetings across disciplines with multiple levels of management
What the job really is

The Master Scheduler at Iovance Biotherapeutics will be responsible for creating and maintaining manufacturing and quality control testing schedules to optimize operations at the Iovance Cell Therapy Center. This role involves collaborating with various departments to ensure alignment with company objectives, monitoring schedule adherence, and adapting plans based on patient demand and operational constraints. The Master Scheduler will also support capacity planning processes and participate in cross-functional meetings to address scheduling challenges.

Things to weigh
  • Less than 5% travel required
  • Potential exposure to lab equipment hazards and chemicals
  • Fast-paced environment may require adjusting workload based on changing priorities
Job score2.6/5
Benefits1/5
Freshness4/5
Career value4/5
Role clarity4/5
Pay transparency0/5

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