Global Quality Program Integration Manager

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 110,000 - 170,000; Full time

Job summary

Scorpion Therapeutics seeks a senior quality program manager to lead global laboratory transformation initiatives within a biopharmaceutical manufacturing context. You will oversee project integration and budget management, coordinating teams across regions to ensure alignment and successful delivery.

The role requires 8+ years in pharma manufacturing or quality with regulatory expertise, plus 5+ years in project management. Hybrid work with ~10% travel expected.

Qualifications

• Bachelor's degree required.
• 8+ years in pharmaceutical manufacturing or quality with regulatory compliance.
• 5+ years of project management experience.

Responsibilities

• Coordinate cross-functional teams regionally and globally to drive program delivery.
• Resolve conflicts and facilitate meetings to maintain alignment across stakeholders.
• Lead process improvements and support business initiatives involving multiple internal and external stakeholders.
• Ensure effective communication and operational excellence across projects.

Skills

Project management

Stakeholder management

Communication

Influencing

Education

Bachelor's degree

Tools

LIMS/ELN

Job description

Role

Manage global quality laboratory transformation initiatives within a biopharmaceutical manufacturing context, overseeing project integration, stakeholder collaboration, and budget management.

Responsibilities

Coordinate cross-functional teams regionally and globally, resolve conflicts, facilitate meetings, and ensure effective communication and operational excellence across projects. Lead process improvements and support business initiatives involving multiple internal and external stakeholders.

Requirements

Bachelor's degree, 8+ years in pharmaceutical manufacturing or quality environment with regulatory compliance expertise, and 5+ years of project management experience. Strong communication, influencing, and stakeholder management skills are essential.

High-Value

Experience with FDA/EMA regulatory requirements, laboratory systems (LIMS/ELN), and managing complex, multi-stakeholder projects in a GMP/GLP setting.

Work Setup

Hybrid, with approximately 10% travel.