What are the responsibilities and job description for the Sr. Validation Engineer (Aseptic/Sterile Manufacturing) position at Sterling Engineering?
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
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
- ~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