Aseptic Manufacturing Tech II - Day Shift (Cell Therapy)

Iovance Biotherapeutics; Philadelphia (Philadelphia County); On-site; USD 55,000 - 75,000; Full time

Job summary

Iovance Biotherapeutics is seeking an Aseptic Manufacturing Technician II to support autologous TIL production in a GMP environment. You will perform suite preparation, material transfers, environmental monitoring, and final product inspection, cryopreservation, and batch completion across rotating shifts.

The role requires a bachelor’s degree (or equivalent) and 0–1 year GMP experience; strong English, MS Office skills, and the ability to work in cleanroom attire, follow GMP/SOPs, maintain

Qualifications

• Bachelor’s degree or equivalent experience.
• 0–1 year GMP manufacturing experience; aseptic technique and transfers a plus.
• Must read, write, and understand English for GMP documentation.
• Proficient in Microsoft Office (Excel, Word, Outlook, Teams).
• Ability to perform arithmetic calculations and basic algebra.
• Ability to work in a fast-paced, team environment and adapt to change.
• Familiar with 21 CFR Part 11 and FDA GMP practices.

Responsibilities

• Understand and execute GMP cell therapy manufacturing processes.
• Complete training and maintain training documentation.
• Adhere to GMP, SOPs, GDP, and Good Documentation Practices.
• Provide operations support: materials stocking, kit prep, room readiness.
• Material transfer, tumor receipt, chain of custody, incubation.
• Run biosafety cabinet (BSC) and perform weight checks, pumps, sealers, incubator use.
• Perform in-suite environmental monitoring and documentation.
• Wear cleanroom PPE and comply with safety SOPs.

Skills

GMP manufacturing

Aseptic technique

BSC operations

Excel

Teamwork

English literacy

Education

Bachelor’s degree

Equivalent experience

Tools

Welders and sealers

BSC operation

Inventory systems

Incubator use

Job description

Iovance Biotherapeutics is seeking an Aseptic Manufacturing Technician II to support autologous TIL production in a GMP environment. You will perform suite preparation, material transfers, environmental monitoring, and final product inspection, cryopreservation, and batch completion across rotating shifts.

The role requires a bachelor’s degree (or equivalent) and 0–1 year GMP experience; strong English, MS Office skills, and the ability to work in cleanroom attire, follow GMP/SOPs, maintain