Aseptic Cell Therapy Technician I — Day Shift B

Iovance Biotherapeutics, Inc.; Philadelphia (Philadelphia County); On-site; USD 28,000 - 41,000; Full time

Job summary

Iovance Biotherapeutics, Inc. is seeking an Aseptic Manufacturing Technician I on Day Shift B (Contract to Hire) in Philadelphia, PA.

Role involves suite prep, material transfer, environmental monitoring, BSC runner duties, and final product handling in a GMP cell therapy setting. The position requires a Bachelor’s degree or equivalent, 0–1 year GMP experience, and strong English literacy for Good Documentation Practices.

Qualifications

• Bachelor’s degree or equivalent experience.
• Minimum 0-1 year of GMP biopharma manufacturing experience, aseptic techniques and related equipment is a plus.
• Must read/write/understand English for Good Documentation Practices.
• Proficiency with Microsoft Excel, Word, Outlook and Teams.
• Able to perform arithmetic with fractions, decimals and percentages; basic algebra/geometry.
• Ability to work in a fast-paced team environment with changing priorities.
• Familiarity with 21 CFR Part 11, GxP and FDA regulations.
• Ability to build relationships quickly and credibly.

Responsibilities

• Develop understanding of GMP cell therapy manufacturing processes.
• Complete training and maintain training docs.
• Adhere to GMP, SOPs and GDP.
• Support suite prep, material transfer and inventory transactions.
• Perform biosafety cabinet runner duties and related tasks.
• Assist in in-suite environmental monitoring and documentation.
• Support production schedule while maintaining priorities.
• Perform other duties as assigned.

Skills

English literacy

Analytical thinking

Math calculations

Problem solving

Team collaboration

GxP knowledge

Education

Bachelor’s degree or equivalent experience

Tools

Microsoft Office Suite

Job description

Iovance Biotherapeutics, Inc. is seeking an Aseptic Manufacturing Technician I on Day Shift B (Contract to Hire) in Philadelphia, PA.

Role involves suite prep, material transfer, environmental monitoring, BSC runner duties, and final product handling in a GMP cell therapy setting. The position requires a Bachelor’s degree or equivalent, 0–1 year GMP experience, and strong English literacy for Good Documentation Practices.