Training Specialist I

5 days ago


Philadelphia, Pennsylvania, United States Iovance Biotherapeutics Inc Full time
Job Title: Training Specialist I

We are seeking a highly skilled Training Specialist I to join our Operations team at Iovance Biotherapeutics Inc. in Philadelphia, PA. As a Training Specialist I, you will play a critical role in developing and delivering training programs for our manufacturing team.

Job Summary:

The Training Specialist I will be responsible for creating and implementing training programs that meet the needs of our manufacturing team. This includes developing training materials, conducting training sessions, and evaluating the effectiveness of our training programs.

Key Responsibilities:
  • Develop and deliver training programs for manufacturing technicians
  • Assist in the creation, review, and improvement of training scripts
  • Present and deliver content to manufacturing technicians
  • Support management in aligning manufacturing processes with technical training
  • Identify training needs and assist in establishing a feedback loop for continuous improvement
  • Assist with drafting SOPs, batch records, deviations, and CAPAs
  • Escalate issues and concerns to area management as needed
Requirements:
  • Bachelor's degree in biology, biochemistry, bioengineering, or related technical field
  • Minimum 2 years of experience in biopharmaceutical GMP manufacturing operations, including experience in cell culture
  • Technical knowledge of aseptic processing in cleanroom environments
  • Experience leading development initiatives, including training, coaching, and mentoring
  • Ability to mentor and provide best practices to new employees
  • Ability to build relationships quickly and provide consistent support to staff
  • Ability to accurately and reproducibly perform arithmetic calculations
  • Proactive, results-oriented, self-starter with strong leadership skills
  • Ability to deal with ambiguity and manage constant change
  • Ability to work successfully in a fast-paced team-oriented setting
  • Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices
  • Excellent presentation skills, both written and verbal
  • Strong computer skills, problem-solving, and attention to detail
  • Familiarity with data and sample management (LIMS/MES)
  • Working knowledge within a Learning Management System (LMS)
Preferred Qualifications:
  • Experience with cell and gene therapy
  • Experience with Master Control
Work Environment:

This position will work in both an office environment and a manufacturing lab setting. Must be able to work in a laboratory setting with various chemical/biochemical exposures, including latex and bleach. Able to work in cleanroom with biohazards, human blood components, and chemicals. Potential exposure to noise and equipment hazards and strong odors.



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