Are you a skilled Commissioning & Qualification (C&Q) Engineer with a passion for sterile drug product manufacturing? We’re seeking a motivated professional to support equipment utilities for filling line systems at a leading biologics facility in Dublin.

Key Responsibilities

• Develop and execute CQV documentation for syringe and vial filling lines, isolators, lyophilizers, and associated equipment.
• Ensure GMP compliance in equipment testing aligned with EU & FDA regulations.
• Manage deviations and implement risk mitigation strategies.
• Lead FAT testing and integrate results into qualification processes.
• Collaborate with cross-functional teams to meet safety, schedule, and quality targets.
• Maintain timely completion of assigned training and documentation.
  
  Qualifications & Experience
  
  
• Bachelor’s degree in a scientific, technical, or engineering discipline.
• 3–5 years of experience in pharmaceutical CQV, ideally with sterile drug product filling line exposure.
  
• Proven track record in CQV lifecycle from design to handover.
  
• Experience with integrated automation systems and electronic validation platforms (e.g., ValGenesis, Kneat).
  

Strong communication and team collaboration skills.

Ready to take the next step in your career?

Apply now to be part of a high-impact project in a cutting-edge biologics environment. For more information or to submit your CV, contact Pawel Jurkiewicz on 0834487062 and let’s start the conversation.

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