Junior Sterilization Validation Analyst (GMP)

Pauwels Consulting; Puurs-Sint-Amands; On-site; EUR 42,000 - 62,000; Full time

Job summary

Pauwels Consulting is seeking a Validation professional to join the GMP-driven validation team in Belgium. You will draft sterilization validation protocols and oversee practical test implementation, ensuring compliance with cGMP and regulatory standards.

You will investigate deviations, maintain GMP documentation, and coordinate activities across the team while supporting transfers to routine programs and participating in site audits for continuous improvement.

Qualifications

• 1+ years of GMP project experience.
• Draft protocols and reports for sterilization validation.
• Plan and monitor validation tests for revalidations and requalifications.
• Investigate deviations and root causes; propose improvements.
• Maintain GMP documentation throughout project lifecycle.
• Coordinate team and communicate progress to stakeholders.
• Support transfer to routine programs through training.
• Participate in site audits and continuous improvement.

Responsibilities

• Draft test protocols for sterilization validation per cGMP and regulatory standards.
• Plan and monitor validation tests for revalidations and requalifications.
• Investigate deviations to identify root causes and improvements.
• Maintain GMP documentation across the project lifecycle.
• Coordinate activities and update stakeholders on progress and deadlines.
• Assist in transferring projects to routine programs via training.
• Contribute to site audits and process optimization initiatives.

Skills

GMP experience

Measurement technology interest

Strong organizational skills

Dutch language

English language

Education

Bachelor/Master in Engineering/Industrial Pharmacy

Tools

PC software proficiency

Job description

Pauwels Consulting is seeking a Validation professional to join the GMP-driven validation team in Belgium. You will draft sterilization validation protocols and oversee practical test implementation, ensuring compliance with cGMP and regulatory standards.

You will investigate deviations, maintain GMP documentation, and coordinate activities across the team while supporting transfers to routine programs and participating in site audits for continuous improvement.