Job Title

Sr. Validation EngineerSterling Engineering Kankakee, Illinois, United States (On-site)Location: Kankakee, ILTitle: Sr. Validation Engineer - Aseptic / Sterile ManufacturingContract Length: 12+ MonthsExperience: ~10 YearsWork Type: Full-time, OnsiteOverviewSeeking 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 documentationRequirements• ~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