The primary responsibility of this role is to assist with the IQ/OQ/PQ of new instruments/equipment in support of manufacturing operations Responsibilities for the (CQV) Commission Qualification Validation Engineerinclude: • Assist with the development of equipment validation protocols (IQ/OQ/PQ) for new instruments and ensure compliance with applicable regulations and guidelines. • Conduct equipment validation testing and generate validation reports. • Provide technical support to manufacturing personnel and troubleshoot any issues related to equipment performance or quality. • Collaborate with cross-functional teams to ensure timely completion of validation activities. • Participate in risk assessments and provide recommendations for risk mitigation. • Assist with the development and implementation of standard operating procedures related to equipment validation and qualification. • Stay up-to-date with industry trends and regulations related to equipment validation and qualification. Qualifications for the (CQV) Commission Qualification Validation Engineer include: • Bachelor's degree in Engineering or a related field. • Minimum of 5+ years of experience in equipment commissioning and validation in a pharmaceutical or medical device manufacturing environment. • Strong knowledge of applicable regulations and guidelines related to equipment validation (e.g., FDA, EU, ICH). • Experience with IQ/OQ/PQ protocols, process validation, and risk assessment. • Excellent problem-solving skills and attention to detail. • Strong communication and interpersonal skills. • Ability to work independently and as part of a cross-functional team Compensation for the (CQV) Commission Qualification Validation Engineer include: • Compensation Range is dependent upon experience • Comprehensive benefits package Keywords GMP, Pharmaceutical Manufacturing, Equipment Qualification, Equipment Commissioning, Equipment Qualification, IQ/OQ/PQ, Comprehensive Benefits Package, Health, Vision, Dental. #LI-ONSITE #LI-DF1