CQV Engineer: Commissioning, Qualification & Validation

IPS-Integrated Project Services; Dublin; On-site; EUR 45,000 - 65,000; Full time

Job summary

A global technical consulting firm in Dublin is seeking a CQV Engineer to support compliance in pharmaceutical facilities. This role involves writing compliance documents, performing field activities, and compiling reports, requiring a Bachelor’s degree in Engineering and at least 5 years of relevant experience. The ideal candidate will have a strong understanding of GMP practices and engage in extensive travel as needed. Join this dynamic team to make a significant impact on project deliveries.

Qualifications

• 5 or more years of relevant experience.
• Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.
• General exposure and experience in a GMP/Validation discipline.

Responsibilities

• Write C/Q/V documents following established standards.
• Perform field/site activities and witness FATs/SATs.
• Compile data and prepare reports for C/Q/V activities.

Skills

cGMP compliance

Field/site activities

Pharmaceutical design and validation

Education

Bachelor of Science in Engineering

Job description

A global technical consulting firm in Dublin is seeking a CQV Engineer to support compliance in pharmaceutical facilities. This role involves writing compliance documents, performing field activities, and compiling reports, requiring a Bachelor’s degree in Engineering and at least 5 years of relevant experience. The ideal candidate will have a strong understanding of GMP practices and engage in extensive travel as needed. Join this dynamic team to make a significant impact on project deliveries.