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Our client – one of the world’s leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better and live longer
You have project management/coordination experience within a QC environment?
Don't hesitate to contact me: email@example.com
Project Manager for QC of the Future for sampling activities & for project related to QC materials management
Manage and execute the programs/projects owned by GASAT (Global Analytical Science and Technology) in the context of automated sampling, sample storage and QC materials management in order to deliver compliance and performance benefits
Establishment of project roadmap, milestones, timeline, resource, risks, governance, interdependencies and other deliveries related planning aspects
Build and present a business case
Overview, coordination and execution of project tasks with proactivity and efficiency
Status/milestones/KPI updates and reports on project progress
Track/record/follow-up of identified risks and mitigation actions
Build stakeholder map and manage stakeholders in terms of communication, engagement, expectation
Organization and logistics for meetings, workshops
Preparation of materials for workshops, presentations, and basic/promotional communication
Recording and documenting of meeting and follow-up of actions
Translate strategy into guidance / instructional documents
Process/system URS compilation
Implementation strategy and plan (pilot and full-scale)
Deployment rollout and follow-up of implementation
Strong PM skills
Experience in pharma & GMP is required. Experience in manufacturing/analytical/QC environment is an advantage.
Experience in sampling and sample and QC materials management is an asset
Experience on automation, digital, in-line monitoring, future technology for sampling
Experience in the coordination of a cross-functional project and handling of multidisciplinary tasks - e.g. interface with representatives from different sites.
Excellent organizational abilities together with managerial and communication skills
Ability to work independently and as part of a multidisciplinary, multi-cultural team within a matrix organization.
Agility in and understanding of highly scientific environment, with GMP rules
Practical experience in writing GMP instructional documents / guidances
Bilingual French/English, written competencies in English
wat bieden wij?
We offer an attractive salary with extra-legal advantages :