Assignment Description
We are looking for an experienced Sub Project Manager
What You Will Work On
- Lead the CIP and Isolator workstream during the project execution phase
- Manage sub-project activities from execution through project completion
- Coordinate suppliers, contractors, and internal project teams
- Drive technical discussions and resolve complex project challenges
- Ensure project delivery according to scope, schedule, budget, and quality objectives
- Develop and maintain project plans, resource plans, and timelines
- Manage project risks using a structured risk-based approach
- Drive risk identification, mitigation, and follow-up activities
- Monitor project progress and report status to project management
- Ensure compliance with GMP standards and project requirements
- Support project documentation and technical decision-making
- Collaborate closely with engineering, quality, validation, and production teams
- Ensure effective communication across all project stakeholders
What You Bring
- Proven experience as a Project Manager or Sub Project Manager within the pharmaceutical industry
- Experience leading at least three GMP-regulated projects from initiation to completion
- Strong experience managing large and complex investment or engineering projects
- Experience managing suppliers and external partners
- Strong knowledge of:
- GMP regulations
- Pharmaceutical manufacturing environments
- Project execution methodologies
- Experience working with risk-based project management
- Strong budget, schedule, and resource management skills
- Excellent communication skills in both Swedish and English
- Ability to work primarily onsite during the execution phase
If this sounds interesting, please send your CV to cv@veritaz.se
