Senior CSA CTOP Coordinator
đ¨ WEâRE HIRING | Senior CSA CTOP Coordinator | Pharma Industry đ¨đ Location: Lebanon, Indiana (100% Onsite)đ Contract Duration: 2+ Yearsđ˘ Visa: Independent Visa OnlyđĽ Interview Process: 2 Virtual Interviewsâ ď¸ Candidates MUST HAVE Pharma / Life Sciences Industry ExperienceWe are actively looking for a Senior CSA CTOP Coordinator with strong experience supporting Construction Turnover Packages (CTOPs) for CSA scopes on large-scale pharmaceutical capital projects.This is a critical onsite role supporting GMP-regulated construction, turnover, commissioning, and validation readiness activities for a major pharmaceutical manufacturing project.đš Key Responsibilities:â Lead CSA Construction Turnover Package (CTOP) activities from mechanical completion through final turnoverâ Manage and track CTOPs aligned with project milestones and turnover strategyâ Coordinate with CSA construction teams for system boundaries, punch list closure, and readiness reviewsâ Work closely with Commissioning, CQV, QA, and Document Control teamsâ Review and validate turnover documentation including:⢠As-built drawings⢠Inspection & test records⢠Material traceability documents⢠Punch list closeout documentationâ Maintain CTOP dashboards, tracking logs, and status reportingâ Participate in walkdowns, turnover meetings, and readiness reviewsâ Ensure compliance with GMP, FDA, and project quality standardsâ Identify turnover risks and proactively drive issue resolutionđš Required Experience:â 8+ years of CSA CTOP / Turnover / Construction Coordination experienceâ MUST HAVE Pharma / Biotech / Regulated Life Sciences project experienceâ Strong understanding of:⢠CSA construction sequencing in GMP environments⢠Mechanical completion vs system turnover⢠Commissioning & Qualification readinessâ Experience working onsite with EPC/EPCM teams and subcontractorsâ Familiarity with GMP documentation standards and audit expectationsâ Experience using CTOP tracking tools and document control systemsâ Preferred:⢠Greenfield pharmaceutical manufacturing project experience⢠Exposure to CQV interfaces for CSA systems⢠EPCM project delivery experienceđŻ Looking for professionals who can drive turnover readiness, coordinate across multidisciplinary teams, and ensure compliant project delivery in highly regulated pharmaceutical environments.đŠ Interested candidates can share:⢠Updated Resume⢠Current Location⢠Visa Status⢠Pharma Project Experience⢠Current & Expected Rate⢠Availability to Joinđ§ Share profiles at: mudit.kumar@thoughtstorm.ca