Validation Engineer

We are actively looking for experienced Commissioning, Qualification & Validation (CQV) professionals for multiple long-term opportunities within the pharmaceutical manufacturing industry.📍 Locations:• Indianapolis, IN• Kansas City, KS• St. Louis, MO• Columbus, OH🔹 Role: Sr. Validation & Compliance Engineer🔹 Experience: 3–10+ Years🔹 Industry: Pharmaceutical / Biopharma ManufacturingKey Responsibilities:✔ Develop and execute IQ/OQ/PQ protocols✔ Commissioning & qualification of equipment, utilities, and facilities✔ Author validation documentation, deviation reports, and summary reports✔ Support GMP compliance and regulatory requirements (FDA/EMA)✔ Collaborate with Engineering, QA, Validation, and Operations teams✔ Participate in CAPA, investigations, and continuous improvement initiativesRequired Skills:• CQV / Commissioning & Qualification experience• Strong understanding of GMP/cGMP environments• Experience with pharmaceutical manufacturing processes• Knowledge of FDA and EMA compliance standards• Excellent documentation and validation experienceIf you are interested or know someone who would be a good fit, feel free to connect or send your updated resume.