Senior Manager of GxP Learning and Development

Allogene Therapeutics; Newark (CA); On-site; USD 140,000 - 190,000; Full time

Job summary

Allogene seeks a Senior Manager of GxP Learning and Development to design, implement, and oversee training programs ensuring GxP compliance and regulatory alignment. You will lead the creation of technical and business training materials and manage LMS operations.

You will collaborate with cross-functional teams in a fast-paced biotech environment, report on training effectiveness, and drive employee growth while maintaining strict regulatory standards at the South San Francisco and Newark, CA

Qualifications

• Bachelor's in Biological Sciences, Chemistry, or Engineering
• minimum 8 years in Pharma/Biotech with 2-3 years of LMS experience
• strong GxP and regulatory knowledge relevant to biotech manufacturing
• excellent communication and interpersonal skills
• ability to work independently in a fast-paced environment

Responsibilities

• Developing training materials
• Managing the Learning Management System (LMS)
• Collaborating with functional managers to identify training needs
• Generating compliance reports

Skills

LMS management

GxP knowledge

Regulatory compliance

Training design

Cross-functional collaboration

Communication skills

Education

Bachelor's in Biological Sciences

Bachelor's in Chemistry

Bachelor's in Engineering

Job description

Role

Senior Manager of GxP Learning and Development at Allogene, responsible for designing, implementing, and overseeing training programs to ensure GxP compliance, regulatory alignment, and support employee growth.

Responsibilities

• Developing technical and business training materials
• Managing the Learning Management System (LMS)
• Collaborating with functional managers to identify training needs
• Generating compliance reports

Requirements

• Bachelor's in Biological Sciences, Chemistry, or Engineering;
• minimum 8 years in Pharma/Biotech with 2-3 years of LMS experience;
• strong GxP and regulatory knowledge relevant to biotech manufacturing;
• excellent communication and interpersonal skills;
• ability to work independently in a fast-paced environment.

Preferred

• Experience with instructional design, training strategy, and cross-functional collaboration.

High Value

• GxP compliance
• biotech/pharma training
• LMS management
• 8+ years industry experience
• focus on regulatory requirements for pharmaceutical manufacturing.

Work Setup

On-site at South San Francisco and Newark, CA; no travel specified.