Iovance Biotherapeutics

Master Scheduler

Iovance Biotherapeutics · Philadelphia, PA

Posted 28 days ago

or apply directly on Iovance Biotherapeutics's site. We never take the application ourselves.

Is this posting real?

This role has been open
28 days
Iovance Biotherapeutics's roles stay open a median of 45 days
Reposted
No
Salary listed
No
0% of Iovance Biotherapeutics's roles list one
Ghost-job risk at Iovance Biotherapeutics
high
23 stale, 1 reposted of 43 open
Hiring momentum
69 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Iovance Biotherapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Iovance Biotherapeutics.

About this role

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.

Our read on this posting2.6out of 5
benefits
1/5
freshness
4/5
career value
4/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Iovance Biotherapeutics as an employer.

What you need

  • 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

Worth weighing

  • Less than 5% travel required
  • Potential exposure to lab equipment hazards and chemicals
  • Fast-paced environment may require adjusting workload based on changing priorities

Summarised from Iovance Biotherapeutics's posting. Read the full original.

Listed by Iovance Biotherapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

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