Sr. Validation Engineer (Aseptic/Sterile Manufacturing)

Sr. Validation Engineer Sterling Engineering Kankakee, Illinois, United States (On-site)

Location:

Kankakee, IL Title:

Sr. Validation Engineer - Aseptic /

Sterile Manufacturing Contract Length:

12+

Months Experience:

~10

Years Work Type:

Full-time, Onsite Overview Seeking an experienced Validation Engineer to support day-to-day validation activities within an aseptic/sterile manufacturing environment. Key Responsibilities

• Provide daily support to site validation team across ongoing manufacturing operations
• Execute validation activities within aseptic liquid processing environments
• Support commissioning, qualification, and validation (CQV) efforts for GMP systems and equipment
• Assist with protocol execution and documentation (IQ/OQ/PQ as applicable)
• Partner with QA, Engineering, and Operations to ensure compliance with cGMP standards
• Support deviation investigations, change controls, and revalidation efforts as needed
• Maintain accurate and compliant validation documentation Requirements
• ~10 years of validation experience in pharmaceutical or biotech environments
• Strong experience in aseptic/sterile liquid manufacturing
• Hands-on CQV experience (equipment, utilities, or processes)
• Working knowledge of cGMP regulations and validation lifecycle
• Ability to operate independently in a fast-paced manufacturing environment