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The Manager, Project Management will lead drug product manufacturing projects, oversee project planning, execution, and stakeholder communication, ensuring timely delivery and adherence to quality standards.

The Training Specialist develops and delivers training materials, supports training compliance, maintains training records, and assists in continuous improvement initiatives for cGMP teams.

Plan mechanical maintenance work, manage documentation, schedule maintenance activities, analyze equipment failures, and communicate with departments to ensure production efficiency.

The Manufacturing Manager leads operations in medical device or drug product manufacturing, ensuring compliance with regulations and efficiency while managing staff and projects.

The Manufacturing Specialist assists in manufacturing tasks, ensuring compliance with regulations and quality standards, while leading process improvements and collaborating with various departments.

The Director of Procurement leads sustainable sourcing efforts, managing supplier relationships, integrating ESG principles, and tracking Scope 3 emissions to drive sustainability initiatives and improve procurement practices.

The Process Reliability Expeditor coordinates tooling, equipment, and parts delivery to operations, manages inventory in CMMS, and assists maintenance teams with tooling issues.

Responsible for monitoring compliance with quality systems through audits, ensuring adherence to PCI Pharma Services standards while providing reporting and support during inspections.

Manage customer projects as the primary contact, ensuring goals are met within budget and regulations. Oversee project planning, budgeting, and client relationships, while leading teams and facilitating communications for project success.

The QA Specialist - Audit will implement GMP auditing, manage supplier qualifications, and ensure compliance with regulations in PCI sites in Ireland.