Overview
We are seeking an experienced Scheduler to support an expanding portfolio of pharmaceutical capital projects across Swiss sites. This role is ideal for professionals with experience in GMP-regulated environments who enjoy managing complex schedules across multiple project types, including warehouse construction, greenfield facilities, and process upgrades.
Language: German-speaking
Start: Early next year
Duration: 6 months+
Project Overview
The role supports a growing programme of capital projects at Swiss pharmaceutical sites, encompassing GMP warehouse builds, greenfield pharma facilities, and process/utility upgrades. Schedules must align with regulatory requirements and the site’s overall master plan.
Main Responsibilities
* Develop and maintain detailed schedules for GMP, warehouse, and greenfield projects
* Ensure sequencing follows CQE (Commissioning, Qualification, Engineering) and validation requirements
* Report progress, risks, and schedule forecasts to site and regional control teams
* Coordinate vendor and contractor timelines within the site master schedule
* Support compliance with internal scheduling and reporting standards
Candidate Profile
* Proven experience scheduling projects in pharma, biotech, or GMP-regulated environments
* Understanding of GMP requirements, CQE workflows, and regulatory-driven milestones
* Experience with greenfield and warehouse projects is advantageous
* Proficient in Primavera P6 and/or MS Project
Competitive and based on experience, skills, and the value you bring to the team
Job function
* Project Management, Engineering, and Strategy/Planning
Industries
* Biotechnology, Engineering Services, and Construction
#J-18808-Ljbffr