Manager, Sterile Drug Product Qa Technical Operations

Bristor Myers Squibb

Cruiserath, Ireland
Hybrid (50% onsite)
Sterile drug product manufacture
Gmp principles biologics
Eu, fda, ich cgmp policies
Bristol Myers Squibb is seeking a Manager for Sterile Drug Product QA Technical Operations at their Cruiserath, Ireland facility. The role involves supporting the start-up of a commercial drug product manufacturing facility, ensuring GMP compliance, and leading quality oversight for sterile drug products

Job Summary

  • This role supports the start-up of a commercial drug product manufacturing facility for its biologic’s commercial portfolio and clinical pipeline.
  • Responsibilities include providing QA Technical Operations support for commercial & clinical sterile drug product manufacture and release activities post start-up.
  • The company offers a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager for Sterile Drug Product QA Technical Operations at their Cruiserath, Ireland facility. The role involves supporting the start-up of a commercial drug product manufacturing facility, ensuring GMP compliance, and leading quality oversight for sterile drug products.

Skills & Requirements

Must-have

  • Sterile Drug Product Manufacture
  • GMP Principles Biologics
  • EU, FDA, ICH cGMP policies
  • Manufacturing unit operations
  • Contamination Control Strategy

Nice-to-have

  • Culture of continuous improvement
  • Operational Excellence initiatives
  • Flexibility to react to changing needs
  • Problem solving and project management

Key Requirements

  • Bachelor/Masters in Engineering, or Science
  • Minimum 5 years' experience
  • Sterile Drug Product Manufacturing experience
  • Annex 1 principles understanding
  • Ability to manage people

Work Rights

Not specified

Tailored Resume

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