Senior CSA CTOP Lead for GMP Turnovers

Accroid Inc; Lebanon (IN); On-site; USD 90,000 - 120,000; Full time

Job summary

Accroid Inc is seeking a Senior CSA CTOP Coordinator to manage Construction Turnover Packages (CTOPs) for CSA scopes on large pharmaceutical capital projects. The ideal candidate will have over 8 years of experience in CSA construction and turnover within regulated life sciences. Responsibilities include leading the CTOP process, coordinating with construction teams, and ensuring compliance with GMP and quality standards. This role requires excellent organizational and communication skills, and familiarity with CTOP tracking tools.

Qualifications

• 8+ years of experience in CSA construction, turnover, or project coordination roles within pharmaceutical, biotech, or regulated life sciences facilities.
• Direct experience managing or supporting CTOPs for CSA scopes on large capital projects.

Responsibilities

• Lead the CSA Construction Turnover Package (CTOP) process from mechanical completion through turnover to Commissioning/Quality.
• Develop, manage, and track CSA CTOPs in alignment with project turnover strategy and schedule milestones.
• Coordinate with CSA construction teams to verify system boundaries, punch list closure, and mechanical completion readiness.

Skills

CSA construction sequencing in GMP environments

Mechanical completion vs. system turnover requirements

Experience working onsite with EPC/EPCM teams

Excellent organizational skills

Communication skills

Stakeholder coordination skills

Tools

CTOP tracking tools

Project management systems

Document control platforms

Job description

Accroid Inc is seeking a Senior CSA CTOP Coordinator to manage Construction Turnover Packages (CTOPs) for CSA scopes on large pharmaceutical capital projects. The ideal candidate will have over 8 years of experience in CSA construction and turnover within regulated life sciences. Responsibilities include leading the CTOP process, coordinating with construction teams, and ensuring compliance with GMP and quality standards. This role requires excellent organizational and communication skills, and familiarity with CTOP tracking tools.