Quality Validation Engineer-Entry Level (Carlsbad)

Job Summary:A leading healthcare technology organization is seeking a Validation Engineer to support validation activities for manufacturing systems, equipment, and processes within a regulated environment. This role will focus on validation documentation, troubleshooting, compliance support, and execution of validation protocols. The ideal candidate will possess strong documentation practices, quality systems knowledge, and the ability to independently manage projects from initiation through completion.Key Responsibilities:• Create, execute, and maintain validation documentation for manufacturing systems, equipment, and processes in compliance with internal quality standards and regulatory requirements• Draft validation protocols, reports, and technical documentation with strong attention to detail and documentation accuracy• Support validation activities related to new product development, process improvements, and system modifications• Evaluate validation results and summarize findings in technical reports and supporting documentation• Perform assessments related to change management activities, including process, system, and document changes• Track validation project progress and maintain accurate project documentation using internal tracking tools• Support internal and external audits by preparing, reviewing, and presenting validation documentation• Troubleshoot validation and quality-related issues while ensuring timely resolution and compliance• Collaborate cross-functionally with engineering, manufacturing, operations, and quality teams• Provide guidance and support to junior team members when neededRequired Qualifications:• Bachelor's degree in Engineering, Life Sciences, or a related technical field• Minimum 2–3 years of experience in validation, quality engineering, or regulated manufacturing environments• Experience writing and executing validation protocols and reports• Strong knowledge of quality systems and documentation practices• Experience supporting change control and validation activities in regulated environments• Strong troubleshooting and problem-solving abilities• Ability to independently manage projects and tasks from beginning to completion• Excellent verbal and written communication skills• Proficiency with Microsoft Office applications and documentation systemsPreferred Qualifications:• Master's degree in a related technical field• Experience supporting manufacturing or medical device validation programs• Experience participating in internal and external audits• Knowledge of regulatory compliance standards and validation requirementsBenefits:The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.Pay Range: $25/hr to $30/hr