Product Security and Tracking Director

hace 4 semanas


Barcelona, Barcelona, España Healthcare Businesswomen's Association A tiempo completo

Job Description Summary

As a key member of the Healthcare Businesswomen's Association, we are seeking a highly skilled Product Security and Tracking Director to lead our global ITOT OT Serialization and Product Tracking organization.

The successful candidate will be responsible for ensuring the establishment, maintenance, and improvement of Serialization and product Security across all control systems, equipment, IT applications, and utilities at our manufacturing sites.

Key Responsibilities:

  1. Manage a global team of senior specialists and Associate directors to drive the program, project, and product delivery to business.
  2. Define, develop, and implement global SPT operations and programs in alignment with our ISC strategy.
  3. Partner with business to drive Transformation programs enabled by technology supporting transformation outcomes.
  4. Measure and drive the business value of transformation initiatives.
  5. Establish key SPT performance indicators to ensure proper service delivery and continuous service improvement.
  6. Support the business to understand fit-for-purpose technical solutions managing requirements with effective cost.
  7. Responsible for recommending, configuring, operating, maintaining, and enhancing relevant Product Security and Tracking systems and tools globally.
  8. Oversee all vendor contracts for Product Security and Tracking and identify cost reduction opportunities.

Requirements:

  1. Bachelor's degree in Computer Science, Information Technology, automation, engineering, or a related field.
  2. Minimum of 7 years of experience in Automation or IT, in a GMP Pharma environment.
  3. In-depth knowledge of automation systems and IT infrastructure.
  4. Strong leadership and team management skills.
  5. Excellent communication and interpersonal skills.
  6. Proven experience in managing budgets and project pipelines.
  7. Familiarity with GMP regulations and compliance standards.
  8. Ability to collaborate with cross-functional teams and key stakeholders.
  9. English fluent.


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