Senior C&Q/CQV Engineer

Job Title: Senior C&Q/CQV Engineer – Pharmaceutical Documentation SMECompany: Intellectt Inc.Location: Indianapolis, INEmployment Type: Long-Term Contract (12+ Months)Job ResponsibilitiesServe as the documentation Subject Matter Expert (SME) across all phases of pharmaceutical Commissioning & Qualification (C&Q/CQV).Conduct field-based system walkdowns and verify equipment and system readiness.Interpret and work extensively with P&IDs to support system verification and commissioning activities.Support system startups and troubleshoot documentation or qualification-related issues.Manage and review C&Q documentation throughout the complete qualification lifecycle.Work closely with engineering and CQV teams to ensure compliance with project requirements.Required QualificationsMinimum 8+ years of pharmaceutical C&Q/CQV experience; 10+ years preferred.Expert-level knowledge of C&Q documentation across all phases of commissioning and qualification.Strong hands-on experience interpreting P&IDs.Direct experience supporting pharmaceutical system startups.Willingness to work in a field-based environment and perform regular system walkdowns.Strong understanding of pharmaceutical commissioning and qualification processes.Previous Lead or Project Management experience is an advantage.Pay Scale-Anticipated hourly pay range: $60-65/hr W2 (Negotiable for candidates with Lead or Project Management experience).BenefitsEmployees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements:Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.Retirement Benefits: A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.Paid Time Off (PTO): No PTO other than that required by applicable state and local laws.