Scientist / Engineer (visual Inspection), Sterile Drug Product Manufacturing, Science & Technology

Bristol Myers Squibb

Cruiserath, Ireland
On-site
Visual inspection process operations and equipment
Sterile drug product manufacturing
Design to ppq of products
Bristol Myers Squibb is seeking a permanent Scientist/Engineer specializing in Visual Inspection for its Sterile Drug Product Manufacturing facility in Cruiserath, Ireland. The role focuses on providing technical expertise for visual inspection processes and ensuring compliance throughout the manufacturing lifecycle

Job Summary

  • Serve as the Technical SME for the Visual Inspection process and related equipment within the new Sterile Drug Product Manufacturing Facility.
  • Oversee all technical aspects from design through successful PPQ and support ongoing operations and global SME activities.
  • Ensure compliance with all Regulatory requirements including Quality (cGDP/GMPs), EHS, and Global Engineering standards.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a permanent Scientist/Engineer specializing in Visual Inspection for its Sterile Drug Product Manufacturing facility in Cruiserath, Ireland. The role focuses on providing technical expertise for visual inspection processes and ensuring compliance throughout the manufacturing lifecycle.

Skills & Requirements

Must-have

  • Visual Inspection process operations and equipment
  • Sterile Drug Product manufacturing
  • Design to PPQ of products
  • Regulatory compliance (cGDP/GMPs, EHS)
  • Technical Transfers and New Product Introduction

Nice-to-have

  • defect classification and particle control
  • Knapp execution and MVI qualification
  • ANSI sampling plans and data trending
  • biologics startup experience
  • MES & SAP systems understanding

Key Requirements

  • Bachelor/Master's in engineering or Science
  • Minimum 5 years' experience in Sterile Drug Product Manufacturing
  • Experience with Visual Inspection and associated equipment
  • Experience with qualification and validation of equipment/processes
  • Experience interacting with regulatory agencies

Work Rights

Not specified

Tailored Resume

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