Associate Director, Reliability And Product Improvement

Century Center

Not specified (likely hybrid based on industry trends).
Bachelor's in engineering degree
10 years pharmaceutical manufacturing experience
Leadership experience in team management
The Associate Director of Reliability and Product Improvement at Century Center is a leadership role focused on enhancing the safety and reliability of marketed combination products in the pharmaceutical sector. The position requires significant experience in engineering, process optimization, and regulatory compliance, as well as strong collaboration skills across various departments

Job Summary

  • This role provides technical leadership to support marketed combination products within CSL's Drug Delivery Systems & Packaging division.
  • The incumbent ensures all sustaining activities comply with international standards including ISO 13485, ISO 14971, and 21 CFR Part 211.
  • CSL Behring is a global biotherapeutics leader driven by a promise to save lives through innovative therapies.

Matching Summary

Match Score: 85

The Associate Director of Reliability and Product Improvement at Century Center is a leadership role focused on enhancing the safety and reliability of marketed combination products in the pharmaceutical sector. The position requires significant experience in engineering, process optimization, and regulatory compliance, as well as strong collaboration skills across various departments.

Skills & Requirements

Must-have

  • Bachelor's in engineering degree
  • 10 years pharmaceutical manufacturing experience
  • Leadership experience in team management
  • Knowledge of cGMP guidelines and validation
  • Understanding of ISO 13485 and ISO 14971

Nice-to-have

  • Experience with process automation
  • Expertise in supplier-related changes
  • Ability to collaborate with CDMOs
  • Strong technical project management skills
  • Deep understanding of regulatory landscape

Key Requirements

  • Bachelor's in mechanical or chemical engineering
  • Minimum 10 years in parenteral or device manufacturing
  • Leadership experience in supervision or management
  • Knowledge of manufacturing processes and validation practices

Work Rights

Not specified

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