Validation Engineer

Job description:Job Summary:The Validation Engineer will be responsible for executing and supporting validation activities within a pharmaceutical manufacturing environment. This is a hands-on, shop-floor–focused role requiring direct involvement with equipment, processes, and systems to ensure compliance with regulatory standards and operational excellence. The ideal candidate will have strong experience in injectable manufacturing and a practical approach to validation execution.Salary range: $70,000 – $80,000 per yearKey Responsibilities:Execute validation activities including IQ, OQ, PQ for equipment, utilities, and processes.Perform hands-on validation work on the shop floor, ensuring protocols are followed and documented accurately.Prepare, review, and execute validation protocols and reports.Support process validation, cleaning validation, and equipment qualification activities.Work closely with manufacturing, engineering, and quality teams to ensure smooth validation execution.Troubleshoot validation issues in real time and implement corrective actions.Ensure compliance with cGMP, FDA, and regulatory requirements.Assist in risk assessments and impact evaluations related to validation activities.Support change control, deviations, CAPA, and revalidation activities.Maintain validation documentation in accordance with company and regulatory standards.Requirements:Bachelor’s degree in Engineering, Pharmacy, or a related field.Minimum of 8+ years of validation experience in the pharmaceutical industry.Mandatory experience in injectable manufacturing.Hands-on experience with equipment qualification and process validation.Solid understanding of cGMP, FDA regulations, and validation lifecycle.Strong problem-solving and troubleshooting skills.Apply now!