Cleaning Validation Engineer

CVE - IRE_1715079154
  • Dublin
  • Contract

Position: Cleaning Validation Engineer
Location: Dublin, Ireland
Contract Length: Initial 6 Months - possibility to extend
Work Structure: Monday - Friday
Pay Rate: Please enquire

Are you a seasoned Cleaning Validation Engineer with a wealth of experience in the Pharmaceuticals Industry?

I am recruiting for a Cleaning Validation Engineer, with experience in bioprocess equipment. The client of ours is expanding their manufacturing and laboratory department, they are seeking x4 Cleaning Validation Consultants for a site in Co. Dublin.

Cleaning Validation Engineer - The Opportunity is great for you because:

  • You will join a company with a track record of developing ground-breaking medicines and vaccines.
  • You will gain invaluable experience at an industry leading bio-pharmaceutical company with a state-of-the-art facility.
  • This client has a diverse product portfolio spanning across a wide range of therapeutic areas, meeting the diverse needs of patients across different disease states around the world.

Cleaning Validation Engineer - Key Responsibilities:

  • Developing and implementing cleaning validation protocols that outline the procedures and criteria for cleaning pharmaceutical manufacturing equipment.
  • Oversee and execute cleaning validation studies and demonstrate the effectiveness of cleaning procedures.
  • Coordinate with analytical laboratories to perform analytical testing on cleaning validation samples.
  • Responsible for documenting all aspects of cleaning validation activities, including study protocols, test results, deviations, corrective actions, and final reports.
  • Conduct risk assessments to identify potential risks associated with cleaning processes, equipment design, product formulations, and manufacturing operations.
  • Participate in continuous improvement initiatives to enhance cleaning validation practices, standard operating procedures (SOPs), and quality systems.

Cleaning Validation Engineer - Qualifications & Requirements:

  • 3+ years of cleaning validation experience within the bio-pharmaceutical or biotechnology industry
  • Experience developing and executing cleaning validation protocols and studies.
  • Experience with vaccine/fill-finish equipment experience is advantageous.
  • Experience with cell culture or biologics equipment.

If you have the expertise and leadership qualities required for this challenging, yet rewarding role, please submit your application including your CV to or press the apply button below.

Jordon Manzo Senior Candidate Consultant I

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