Manager, GLP Compliance

Scorpion Therapeutics; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

Scorpion Therapeutics seeks a Manager of GLP Compliance to support laboratory operations in a biopharma setting focused on autoimmune disease therapies, including cell and gene therapies. You will ensure GLP across lab activities, develop QC processes, and support audits while managing documentation and providing GLP training.

The role emphasizes collaboration with Clinical Operations, Regulatory Affairs, and vendor partners to maintain inspection readiness and drive a culture of quality in a

Qualifications

• Bachelor's in Life Sciences or related field.
• At least 2 years of experience in biopharma/lab operations in GxP environments.
• Familiarity with GLP, GCP, ICH guidelines, and FDA regulations.

Responsibilities

• Ensure GLP compliance across laboratory activities.
• Develop and improve quality control processes.
• Support audits and inspections.
• Manage documentation.
• Provide GLP training.
• Promote continuous quality improvement.
• Collaborate with Clinical Operations, Regulatory Affairs, and vendors to maintain inspection readiness.

Skills

GLP compliance

Quality control

Documentation management

Audit readiness

Cross-functional collaboration

Education

Bachelor's in Life Sciences or related field

Job description

Role

Manager, GLP Compliance supporting laboratory operations in a biopharma setting focused on autoimmune disease therapies, including cell and gene therapy.

Responsibilities

• ensure GLP compliance across laboratory activities
• develop and improve quality control processes
• support audits and inspections
• manage documentation
• provide GLP training
• promote continuous quality improvement
• Collaborate with cross-functional teams such as Clinical Operations, Regulatory Affairs, and vendors to maintain inspection readiness and foster a culture of quality.

Requirements

• Bachelor's in Life Sciences or related field
• at least 2 years of experience in biopharma/lab operations within GxP environments, supporting document control, and familiarity with GLP, GCP, ICH guidelines, and FDA regulations.

Preferred

• experience with cell and gene therapy.

High-value

supporting GLP compliance in a clinical-stage biotech advancing autoimmune therapies, including CAR T-cell products, with a focus on regulatory adherence, documentation, audit readiness, and cross-disciplinary collaboration.

Work Setup

remote based in Philadelphia, PA.