Validation Engineer

Job Summary We are seeking a Validation Engineer to support validation activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on equipment, utilities, and process validation, ensuring compliance with regulatory requirements and supporting ongoing manufacturing operations. Job Title: Validation Engineer Location: Concord, NC (Onsite) Duration: Long Term Key Responsibilities Execute and support equipment, utility, and process validation activities (IQ, OQ, PQ) Develop and review validation protocols, reports, and supporting documentation Ensure compliance with GMP, FDA, and regulatory requirements Perform risk assessments and support validation strategies Collaborate with Engineering, Quality, and Manufacturing teams Support deviation investigations, CAPA, and change control activities Assist with commissioning and qualification (CQV) activities Maintain accurate and compliant documentation Required Qualifications Bachelor s degree in Engineering, Science, or related field 3 7+ years of experience in validation within pharmaceutical or biotech industry Hands‑on experience with IQ/OQ/PQ and validation documentation Strong understanding of GMP and regulatory compliance Experience with equipment and/or utility validation #J-18808-Ljbffr Stark Pharma