Manager, Product Quality

Scorpion Therapeutics; Indiana (PA); On-site; USD 66,000 - 169,000; Full time

Job summary

Scorpion Therapeutics in the United States is seeking a Manager of Product Quality to oversee quality activities for development and commercial-stage products, ensuring compliance, performance, and continuous improvement throughout the product lifecycle.

The role collaborates with Clinical Operations, Manufacturing, Regulatory, and Supply Chain to maintain GMP standards, manage investigations, and support regulatory submissions; offers a competitive salary and comprehensive benefits.

Qualifications

• BS/MS in Life Sciences is required.
• 5-10 years pharmaceutical quality experience.
• Knowledge of GMP manufacturing and quality systems.
• Authorized to work full-time in the U.S.

Responsibilities

• Lead product quality for assigned programs; investigate complaints; support clinical operations and manufacturing campaigns; review deviations, investigations, CAPAs, and change controls; analyze quality trends; develop risk assessments; support regulatory inspections.

Skills

GMP knowledge

Quality systems

Education

BS/MS in Life Sciences

Job description

Role

Manager of Product Quality overseeing quality activities for development and commercial-stage products, ensuring compliance, performance, and continuous improvement throughout the product lifecycle.

Responsibilities

• Lead product quality for assigned programs, investigate product complaints, support clinical operations and manufacturing campaigns, review deviations, investigations, CAPAs, and change controls, analyze quality trends, develop risk assessments, and support regulatory inspections and audits.

Requirements

• BS/MS in Life Sciences
• 5-10 years pharmaceutical quality experience
• Knowledge of GMP manufacturing and quality systems
• Authorized to work full-time in the U.S.
• Additional preferences include problem-solving skills, technical depth, and interest in AI and digital innovation.

High Value

quality oversight across pharma development and manufacturing, compliance with GMP, support for regulatory submissions, cross-functional collaboration with Clinical Operations, Supply Chain, Manufacturing, and Regulatory teams.

Work Setup

• Full-time
• Based in the U.S.
• Salary range of $66,000 - $169,400
• Plus bonus and comprehensive benefits