Pharma CQV Engineer: IQ/OQ/PQ Expert

Capgemini Engineering; Diegem; On-site; EUR 65,000 - 95,000; Full time

Job summary

Capgemini Engineering is seeking an experienced Commissioning, Qualification and Validation Engineer for the pharmaceutical industry in Diegem, Belgium. You will join expert teams to ensure compliance and quality of pharmaceutical facilities and equipment.

You will develop and execute qualification/validation protocols, perform CQV activities in line with GMP, and document results with detailed reports. You will collaborate across disciplines and contribute to corrective actions as deviations

Qualifications

• Engineering degree in pharmaceutical engineering, biochemistry, process engineering or related field.
• Completed at least one internship in the pharmaceutical industry or in a similar regulated environment.
• Knowledge of GMP, pharmaceutical regulations, IQ/OQ/PQ methodologies.
• Fluent in English with a good level of Dutch (written and spoken).

Responsibilities

• Participating in the development and execution of qualification and validation protocols for pharmaceutical equipment and systems
• Performing commissioning, qualification and validation (CQV) activities in accordance with GMP and pharmaceutical regulations
• Executing IQ/OQ/PQ testing to verify that systems and equipment are installed correctly and operate as intended
• Collaborating with multidisciplinary teams to ensure facility compliance with regulatory requirements and client specifications
• Documenting test results and writing detailed technical reports
• Identifying deviations and participating in the implementation of corrective actions.

Skills

GMP knowledge

English proficiency

Dutch language

Education

Engineering degree (pharmaceutical engineering or related)

Tools

IQ/OQ/PQ methodologies

Job description

Capgemini Engineering is seeking an experienced Commissioning, Qualification and Validation Engineer for the pharmaceutical industry in Diegem, Belgium. You will join expert teams to ensure compliance and quality of pharmaceutical facilities and equipment.

You will develop and execute qualification/validation protocols, perform CQV activities in line with GMP, and document results with detailed reports. You will collaborate across disciplines and contribute to corrective actions as deviations