Cleaning Validation Engineer TPM6081

Tandem Project Management Ltd.; Cork; Hybrid; EUR 60,000 - 80,000; Full time

Job summary

Tandem Project Management Ltd. is assisting a global biopharmaceutical company in Cork to hire a Cleaning Validation Engineer.

You will work with the process and cleaning validation team to ensure compliance, product quality, and reliability across manufacturing operations. Responsibilities include cleaning validations and verification programs for commercial and clinical solid oral dose products, performing calculations and assessments, sampling equipment, monitoring validated processes,

Qualifications

• BSc in Engineering or Science required.
• 5 years' experience in pharmaceutical/biopharmaceutical manufacturing.
• Experience in cleaning validation is essential.
• Knowledge of qualification/validation requirements and good documentation practices.

Responsibilities

• Work on cleaning validations and cleaning verification programs for commercial and clinical solid oral dose products.
• Perform cleaning calculations and assessments along with all associated protocols and reports.
• Sampling manufacturing and packaging equipment for analysis.
• Routine monitoring of validated cleaning processes.
• Assisting in any associated cleaning deviations.
• Any other ad hoc project deliverables.

Skills

Validation knowledge

Documentation accuracy

Analytical thinking

Education

BSc in Engineering or Science

Job description

Summary:

Our client is a global biopharmaceutical company in Cork is looking to hire a Cleaning Validation Engineer. The candidate would be working with the process and cleaning validation team.

Responsibilities:

• Working on both cleaning validations and cleaning verification programs for commercial and clinical solid oral dose products
• Performing cleaning calculations and assessments along with all associated protocols and reports
• Sampling manufacturing & packaging equipment for analysis
• Routine monitoring of validated cleaning processes
• Assisting in any associated cleaning deviations
• Any other ad hoc project deliverables.

Qualifications & Experience:

• Minimum - BSc in either Engineering or Science
• 5 years' experience supporting a pharmaceutical / biopharmaceutical manufacturing site.
• Previous experience in cleaning validation is essential
• Knowledge of qualification/validation requirements and good documentation practices.