Analytical Sciences and Technology Specialist I

Iovance Biotherapeutics • Philadelphia, PA

11d • Onsite

About The Position

The ASaT Specialist is accountable for the technical development of quality control methods and processes, method and instrument validations, and technical transfers related to Analytical and/or Microbiological quality control testing of products, raw materials, and packaging components at the site. This role is also responsible for operating and maintaining quality control instrumentation in compliance with cGMP/FDA regulations, Iovance standard operating procedures, and policies. Given the nature of the process, this role also necessitates expertise in quality control techniques, analytical instrumentation, sterility principles, and an understanding of radiation safety standards.

Requirements

• A minimum of a bachelor’s degree in biology, Biochemistry, Microbiology, Chemistry, or related scientific field and 1-3 years of experience is required.
• Solid understanding and functional knowledge with hands-on experience with Flow Cytometry, Cell-based ELISA, cell culture (primary cells and cell lines), and molecular assays.
• Proficient in performing technical writing (e.g., test methods, SOPs, protocols, etc.)
• Successfully interface with multi-disciplined teams.
• Extremely detail-oriented with strong technical skills.
• Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity.
• High level of ownership and accountability.
• Demonstrate a sense of urgency; ability to recognize time sensitivity.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)

Nice To Haves

• Master’s degree with four years of experience.
• Experience with cell therapy products is a plus.

Responsibilities

• Executes testing for method and instrument implementation and qualification/validation protocols.
• Supports Phase II LIR OOS/OOT investigational testing.
• Responsible for the timely completion of required, including SOPs, aseptic techniques, gowning, testing, and EHS.
• Prepares applicable documents, forms, and records, such as method or instrument qualification/validation records, and follows Good Documentation Practices.
• Supports internal and external Audits and Inspections, if needed.
• Adheres to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
• Performs miscellaneous duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level