Iovance Biotherapeutics

Specialist I, Quality Control Compliance ( Contract to Hire )

Iovance Biotherapeutics · Philadelphia

Posted about 3 months ago

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

Is this posting real?

This role has been open
82 days
Iovance Biotherapeutics's roles stay open a median of 83 days
Reposted
No
Salary listed
No
0% of Iovance Biotherapeutics's roles list one
Ghost-job risk at Iovance Biotherapeutics
high
43 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
2026-10-25

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 Quality Control Compliance Specialist I will manage Quality Control documentation and data, including issuing testing forms and maintaining data storage. The role involves tracking batches in LIMS, generating Certificates of Analysis, and assisting with quality record management. This position requires attention to detail and the ability to handle multiple priorities in a fast-paced environment, working on-site from Wednesday to Saturday.

Our read on this posting1.8out of 5
benefits
1/5
freshness
1/5
career value
3/5
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

  • Bachelor’s degree in a relevant discipline (biological sciences or equivalent)
  • Minimum (3) years of experience in the biopharmaceutical industry within a cGMP Quality Control role
  • Good understanding of cGMP quality records, QC testing/LIMS, and quality metrics
  • Extremely detail-oriented with strong analytical, written, and verbal communication skills
  • Ability to effectively manage multiple priorities involving aggressive timelines
  • Demonstrate sense of urgency and ability to recognize time sensitivity

Nice to have

  • Experience with cell and/or gene therapy products
  • Ability to interface with multi-disciplined teams in a global setting
  • Flexible and adaptable style with eagerness to take on challenges

Worth weighing

  • 100% on-site work
  • Wednesday to Saturday shift may not suit all candidates
  • Potential exposure to noise and equipment hazards in the work environment

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

Listed by Iovance Biotherapeutics on their greenhouse job board, last confirmed open on 2026-10-25. PitchMeAI is not the employer.

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