Mgr, Quality Assurance

Newyorkbioconnect

Carlow, Ireland
Hybrid
Cgmp compliance
Data integrity principles
Sterile manufacturing experience
You will provide expert Quality input and subject matter insight across three manufacturing suites, supporting timely and effective issue resolution

Job Summary

  • You will provide expert Quality input and subject matter insight across three manufacturing suites, supporting timely and effective issue resolution.
  • Foster consistent product quality and patient safety by supporting batch review and Product Safety Incident Management activities.
  • Champion a safe, compliant, high-performance, and inclusive culture within the team.

Matching Summary

You will provide expert Quality input and subject matter insight across three manufacturing suites, supporting timely and effective issue resolution.

Skills & Requirements

Must-have

  • cGMP Compliance
  • Data Integrity principles
  • Sterile manufacturing experience
  • Quality input and subject matter insight

Nice-to-have

  • High-performance and inclusive culture
  • Continuous Improvement projects
  • Flexible working where possible

Key Requirements

  • Degree or higher in a Science-based discipline
  • Minimum of 5 years’ experience in the pharmaceutical industry
  • Sterile manufacturing experience is essential
  • Existing People Management experience is a distinct advantage

Work Rights

Not specified

Tailored Resume

Cover Letter