GMP Training & LMS Specialist I

Iovance Biotherapeutics, Inc.; Philadelphia (Philadelphia County); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Iovance Biotherapeutics, Inc. in Philadelphia, PA, seeks a Technical Learning Specialist I to support the GMP training administration program. Your role includes managing the LMS, delivering training, and ensuring records and reports meet quality standards.

You will collaborate with cross-functional teams, support onboarding, and help implement new LMS features while adhering to GMP and GDP guidelines in a fast-paced cell therapy environment.

Qualifications

• Bachelor's degree in Life Sciences or equivalent with 2+ years in GMP training documentation.
• Familiar with document change management and FDA quality systems.
• Experience with an LMS/DMS (MasterControl is a plus).
• Strong attention to detail and data integrity.
• Proficient in Word and Excel.

Responsibilities

• Supports LMS training program, with accurate reports and metrics for groups and leadership.
• Maintains qualification training records for site personnel in the LMS.
• Administers and assigns training; creates LMS infrastructure (courses, job codes).
• Supports new hire onboarding and orientation in the LMS.
• Provides LMS end-user support and troubleshoots simple issues.
• Leads training-related projects with cross-functional teams to closure.
• Ensures GMP, GDP, and SOP compliance in training materials and documentation.
• Participates in training content improvements and SOP revisions.

Skills

LMS Admin

Documentation

Training Delivery

GMP Knowledge

Data Integrity

MS Word

MS Excel

Cross-functional

Attention to Detail

Education

B.S. Life Sciences

Tools

MasterControl

LMS

MS Word

MS Excel

Job description

Iovance Biotherapeutics, Inc. in Philadelphia, PA, seeks a Technical Learning Specialist I to support the GMP training administration program. Your role includes managing the LMS, delivering training, and ensuring records and reports meet quality standards.

You will collaborate with cross-functional teams, support onboarding, and help implement new LMS features while adhering to GMP and GDP guidelines in a fast-paced cell therapy environment.