Remote GLP Compliance Manager — Quality & Lab Oversight

Valid8 Financial, Inc.; Philadelphia (Philadelphia County); On-site; USD 120,000 - 165,000; Full time

Benefits offered by this job

Competitive benefits

Stock option plans

PTO

Job summary

Cabaletta Bio is seeking a Manager, GLP Compliance to oversee quality systems across laboratory operations supporting clinical development in the Philadelphia area. The role emphasizes GLP compliance, GxP training, documentation management, and inspection readiness to ensure data integrity and regulatory adherence.

The position requires a Bachelor’s degree in a relevant scientific field and 2+ years in GxP environments, with strong collaboration skills to work with Clinical Operations,

Qualifications

• Bachelor's degree in Biology, Chemistry, Life Sciences, or related scientific discipline.
• Minimum of two (2) years of hands‑on experience in biopharmaceutical operations, laboratory operations, quality operations, or related GxP environment.
• Minimum of one (1) year of experience supporting Document Control within a GxP environment, including TMF documentation.

Responsibilities

• Ensure GLP compliance across internal, central, and local laboratory activities.
• Develop, implement, and maintain quality control processes and procedures.
• Assist in audits and inspection readiness, including documentation and responses.
• Maintain controlled laboratory documents, SOPs, protocols, and quality records.
• Support GLP training and foster a culture of quality and compliance.
• Collaborate with cross‑functional stakeholders to implement process improvements.

Skills

GLP Compliance

GxP environment

Quality Systems

Documentation Management

Training & Compliance

Cross-functional collaboration

Attention to detail

Microsoft Office

Education

Bachelor's degree in Biology, Chemistry, Life Sciences or related field

Tools

TMF documentation systems

QMS software

Job description

Cabaletta Bio is seeking a Manager, GLP Compliance to oversee quality systems across laboratory operations supporting clinical development in the Philadelphia area. The role emphasizes GLP compliance, GxP training, documentation management, and inspection readiness to ensure data integrity and regulatory adherence.

The position requires a Bachelor’s degree in a relevant scientific field and 2+ years in GxP environments, with strong collaboration skills to work with Clinical Operations,