Remote Global QMS Director – Compliance & Inspection

Scorpion Therapeutics; United States; Remote; USD 180,000 - 250,000; Full time

Benefits offered by this job

Remote work

Travel opportunities

Job summary

Scorpion Therapeutics is seeking a leader to drive global QMS functions in a biopharma manufacturing context, ensuring compliance, inspection readiness, and ongoing improvement.

The role oversees document control, training, CAPA, deviations, change control, and risk management, leads eQMS validation, supports regulatory inspections, and embeds quality in business processes while tracking system performance; remote with monthly travel to Norwood, MA.

Qualifications

• Bachelor/Master/Doctorate in Life Sciences.
• 10+ years in GxP biotech/pharma.
• Expertise with FDA/EMA/MHRA regulations.
• eQMS validation/maintenance and audit experience.

Responsibilities

• Oversee document control, training, CAPA, deviations, change control, and risk management.
• Manage end-to-end lifecycle of quality documentation.
• Lead implementation and validation of eQMS.
• Support regulatory inspections and audits.
• Embed quality in business processes and drive system performance metrics.

Skills

GxP regulations

Audit experience

Cross-functional collaboration

Education

Life Sciences degree (BSc/MSc/PhD)

Tools

Veeva

MS Office

Job description

Scorpion Therapeutics is seeking a leader to drive global QMS functions in a biopharma manufacturing context, ensuring compliance, inspection readiness, and ongoing improvement.

The role oversees document control, training, CAPA, deviations, change control, and risk management, leads eQMS validation, supports regulatory inspections, and embeds quality in business processes while tracking system performance; remote with monthly travel to Norwood, MA.