Senior CSA CTOP Coordinator Onsite

Job Title: Senior CSA CTOP CoordinatorLocation: Lebanon, INOnite 2 Virtual InterviewsContract Length: 2+ Years8+ years CTOP experience, some pharma requiredSpecific to CSA scopeJob DescriptionPosition OverviewThe Senior CSA CTOP Coordinator is responsible for managing Construction Turnover Packages (CTOPs) for CSA scopes on large scale pharmaceutical capital projects. This role serves as the link between construction, quality, commissioning, and project controls to ensure CSA systems are completed, documented, and turned over in compliance with GMP, project sequencing, and validation readiness requirements.The ideal candidate has hands on experience supporting CTOP execution on regulated life sciences projects and understands how CSA turnover directly impacts commissioning, qualification, and subsequent validation activities.Key ResponsibilitiesLead the CSA Construction Turnover Package (CTOP) process from mechanical completion through turnover to Commissioning/QualityDevelop, manage, and track CSA CTOPs in alignment with project turnover strategy and schedule milestonesCoordinate with CSA construction teams to verify system boundaries, punch list closure, and mechanical completion readinessWork cross functionally with Commissioning, CQV, QA, and Document Control to support timely and compliant system handoverReview And Validate CSA Turnover Documentation, IncludingAs built drawingsInspection and test recordsMaterial traceability and certificationsPunch list and deficiency closeout documentationMaintain CTOP tracking logs and dashboards; provide regular status updates to project leadershipParticipate in turnover meetings, walkdowns, and system readiness reviewsEnsure turnover packages meet GMP, FDA, and project specific quality requirementsIdentify risks to turnover readiness and proactively drive resolution with construction and project teamsSupport audit readiness related to CSA construction and turnover documentationRequired Qualifications8+ years of experience in CSA construction, turnover, or project coordination roles within pharmaceutical, biotech, or regulated life sciences facilitiesDirect experience managing or supporting CTOPs for CSA scopes on large capital projectsStrong Understanding OfCSA construction sequencing in GMP environmentsMechanical completion vs. system turnover requirementsHow CSA readiness affects commissioning and qualificationExperience working onsite with EPC/EPCM teams and multiple subcontractorsFamiliarity with GMP documentation standards and audit expectationsProficiency with CTOP tracking tools, project management systems, and document control platformsExcellent organizational, communication, and stakeholder coordination skillsPreferred QualificationsExperience on large greenfield pharmaceutical manufacturing projectsPrior exposure to CQV interfaces for CSA systems (rooms, finishes, envelopes, etc.)Background working under EPCM delivery models