Pharma Data Integrity Engineer – GMP, CSV & ALCOA+

Capgemini Engineering; Utrecht; On-site; EUR 40,000 - 59,000; Full time

Benefits offered by this job

Mobility allowance

8% holiday allowance

26 vacation days

Home office allowance

Laptop and SIM for work

Job summary

Capgemini Engineering is seeking a Data Integrity Engineer for a client in the pharmaceutical sector in Leiden. You will optimize data storage, minimize data vulnerability, and collaborate with Capgemini and client representatives to define data processes, perform risk assessments, and drive risk mitigation initiatives.

The role involves working with production equipment, creating Visio data flow charts, and ensuring ALCOA+ data integrity across processes.

Qualifications

• Bachelor’s or Master’s degree in a related technical field.
• Solid understanding of GMP regulations and industry standards.
• Knowledge of ALCOA+ principles.
• Hands-on experience with CSV is valuable.
• Experience in risk assessments and documentation.

Responsibilities

• Define data processes and risk mitigation initiatives with client and Capgemini teams.
• Prepare risk assessments and maintain documentation.
• Work with production equipment and data storage optimization.
• Develop data flow charts based on Visio and ensure data integrity.

Skills

GMP knowledge

ALCOA+ principles

CSV experience

Risk assessment

Documentation skills

Education

Food Technology

(Bio)Process Technology

Chemistry

Tools

Visio

Job description

Capgemini Engineering is seeking a Data Integrity Engineer for a client in the pharmaceutical sector in Leiden. You will optimize data storage, minimize data vulnerability, and collaborate with Capgemini and client representatives to define data processes, perform risk assessments, and drive risk mitigation initiatives.

The role involves working with production equipment, creating Visio data flow charts, and ensuring ALCOA+ data integrity across processes.