Sub Project Manager GMP Projects 18367
Core
Lead CIP and Isolator workstreams for pharmaceutical manufacturing projects, managing execution from initiation to completion while ensuring GMP compliance.
Role type
Sub Project Manager (Pharmaceutical Engineering)
Builds
Pharmaceutical manufacturing facilities (CIP and Isolator systems)
Domain
Pharmaceutical manufacturing / Engineering construction
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP regulations, Pharmaceutical manufacturing environments, Project execution methodologies, Risk-based project management, Budget management, Schedule management, Resource management, Supplier management, Technical decision-making
Preferred skills
Leading GMP-regulated projects, Managing large complex investment projects, Managing external partners
Technologies
None stated
Responsibilities
Lead CIP and Isolator workstreams, Manage sub-project activities, Coordinate suppliers and contractors, Drive technical discussions, Ensure project delivery against scope/schedule/budget, Develop and maintain project plans, Manage project risks, Monitor project progress, Ensure GMP compliance, Support project documentation, Collaborate with engineering and quality teams
Seniority
Experienced, hands-on IC
