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The Manufacturing Systems and Projects Leader is responsible for leading manufacturing projects and systems-related Product Lifecycle Management (PLM) activities across the Cardiff site. This position reports to the Senior Operations Manager and is part of the Operations team located in Cardiff and will be an on-site role.
Job Responsibility:
Own and manage the systems-related elements of PLM activities for Cardiff-assigned products across the full product lifecycle, including development, release, change, sustainment, and obsolescence
Chair the Cardiff product Engineering Change Control Boards (ECCB), ensuring engineering changes are prepared, reviewed, approved, implemented, and closed in accordance with Cytiva procedures
Act as the Cardiff subject matter expert for MAGIC, ensuring accurate configuration management, BOM structures, document control, and lifecycle state management
Manage and support the integration between MAGIC PLM and Oracle ERP, ensuring correct transfer of product structures, costs, revisions and change status. Partner with Engineering, Quality, Manufacturing, Supply Chain, and IT teams to ensure PLM and ERP data integrity, compliance, and manufacturing readiness
Act as manufacturing project leader for site portfolio projects, including leadership of VPM (Visual Project Management), project team daily management and change management
Requirements:
Academic qualification, or equivalent practical experience, in Engineering, Manufacturing, or a related discipline
Experience in MAGIC Product Lifecycle Management and engineering change control within a regulated environment
Practical experience working with ERP systems, preferably Oracle ERP, including PLM–ERP data integration for BOMs, revisions, and change implementation
Experience of working within a QMS, preferably Veeva, to manage process deviations, quality documentation and change control
Experience in project leadership, including oversight of multidisciplinary project teams, task coordination, and effective use of daily management systems to track progress
Nice to have:
Experience in medical, biotechnology, or life sciences environments
Familiarity with quality and regulatory standards such as ISO 13485 or FDA QSR