Senior Associate Director, GMP Validation & Facilities

Scorpion Therapeutics; California (MD); On-site; USD 150,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking an Associate Director of Validation within Facilities and Engineering to oversee site-wide validation programs supporting GMP compliance in a pharmaceutical setting.

You will lead validation strategies for facilities, equipment, and processes, manage lifecycle activities from commissioning to audits, and ensure rigorous documentation and system compliance across sites.

Qualifications

• 10-12 years in validation management, engineering, or capital projects in regulated industries.
• Extensive GMP, FDA knowledge.
• Strong project management, analytical, and communication skills.

Responsibilities

• establishing validation strategies aligned with cGMP
• leading validation projects for facilities, equipment, and processes
• ensuring documentation and system compliance
• managing validation lifecycle activities from commissioning to qualification and validation audits

Skills

Project management

Analytical skills

Communication skills

Leadership

Education

Bachelor's in Engineering or related field

Job description

Scorpion Therapeutics is seeking an Associate Director of Validation within Facilities and Engineering to oversee site-wide validation programs supporting GMP compliance in a pharmaceutical setting.

You will lead validation strategies for facilities, equipment, and processes, manage lifecycle activities from commissioning to audits, and ensure rigorous documentation and system compliance across sites.