Validation engineer

Senior Commissioning, Qualification, and Validation (CQV) EngineerThis role offers the opportunity to work on cutting-edge automated inspection systems and contribute to meaningful advancements in pharmaceutical manufacturing.About the Role:As a Senior CQV Engineer, you'll play a key role in executing commissioning and qualification activities for advanced automated equipment. You'll collaborate with cross-functional teams, maintain project documentation, and ensure compliance with regulatory and quality standards.Key Responsibilities:Lead commissioning and qualification efforts for automated syringe inspection systems.Prepare, review, and execute validation protocols (URS, IQ, OQ, PQ).Track project progress, maintain documentation logs, and manage open items.Conduct risk and impact assessments in collaboration with project teams.Ensure alignment with project timelines and deliverables.What We're Looking For:Willingness to work on-site in Bloomington, IN.Bachelor's degree in engineering or a related field (or equivalent experience).5+ years of experience in CQV, particularly with automated inspection systems.Strong understanding of capital equipment implementation and validation processes.Familiarity with GMP standards and Good Documentation Practices.Proficiency in Microsoft Word (especially for technical documentation), Excel, and PowerPoint.Excellent communication and problem-solving skills.Experience with machine safety, Ethernet networking, and power system design is a plus.Benefits Overview:Competitive salary with performance-based incentivesHealth, dental, and vision insuranceCompany-paid life and disability coverageHealth Savings Account (HSA) and Flexible Spending Accounts (FSA)401(k) with employer matchPaid time off, holidays, and sick leaveTuition reimbursement and professional development supportParental leave and bereavement benefitsEmployee referral and recognition programsTeam-building events and a collaborative work culture