Lab CQV Engineer: Qualified Lab Equipment & Compliance

Arcadis; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

Arcadis is seeking a Lab CQV Engineer to support laboratory equipment projects across Drug Substance, Vaccines, Bioprocessing and Parenteral units. You will provide engineering SME expertise to ensure IQ/OQ/PQ, commissioning and qualification meet local and regulatory requirements.

The role focuses on bench-top and analytical lab equipment, Nova BioProfile FLEX systems, and collaborates with Quality, Automation, IT and equipment vendors to deliver compliant solutions.

Qualifications

• B.Sc./B.Eng. in engineering, science or related field.
• 2-5 years GMP bioprocess or regulated lab experience.
• Experience delivering CQV across lifecycle.
• Knowledge of GMP, data integrity, change control and risk-based qualification.

Responsibilities

• Lead or support laboratory equipment CQV projects across the lifecycle.
• Develop, review and execute IQ/OQ/PQ protocols and qualification reports.
• Coordinate vendor activities for installation, calibration and commissioning.
• Ensure compliance with GMP and regulatory requirements.
• Maintain validated state through calibration and maintenance reviews.
• Collaborate with Engineering, Quality, Automation, IT and vendors.

Skills

CQV experience

GMP knowledge

Cross-functional teamwork

Documentation skills

Communication skills

Risk-based qualification

Education

B.Sc./B.Eng. in engineering or science

Tools

Nova BioProfile FLEX

Laboratory equipment CQV

Job description

Arcadis is seeking a Lab CQV Engineer to support laboratory equipment projects across Drug Substance, Vaccines, Bioprocessing and Parenteral units. You will provide engineering SME expertise to ensure IQ/OQ/PQ, commissioning and qualification meet local and regulatory requirements.

The role focuses on bench-top and analytical lab equipment, Nova BioProfile FLEX systems, and collaborates with Quality, Automation, IT and equipment vendors to deliver compliant solutions.