Requalification/Revalidation Engineer

EFOR; Geel; On-site; EUR 60,000 - 90,000; Full time

Job summary

EFOR in Geel, Belgium is seeking an experienced Requalification/Revalidation Engineer to join our remediation program. You will support requalification of critical equipment (autoclaves, washers, CTUs) and contribute to qualification and validation of biologics process equipment.

The role requires GMP understanding, strong documentation skills, and the ability to adapt to changing project scopes while delivering high-quality validation outcomes in a state-of-the-art biologics manufacturing

Qualifications

• Experience with equipment requalification and/or revalidation (autoclaves, washers, CTUs).
• Experience with qualification/validation in biologics manufacturing is a strong plus.
• Good understanding of GMP and regulatory requirements.
• Strong documentation and technical writing skills.
• Ability to adapt to changing project scopes and priorities.

Responsibilities

• Support the requalification of critical equipment (autoclaves, washers, CTUs) as part of remediation.
• Assist in the qualification and validation of biologics process equipment, with potential to support both activities as needed.

Job description

Are you an experienced validation professional ready for your next challenge? We are seeking a Requalification/Revalidation Engineer to join the team at our Geel site in Belgium.

About the Role:

As a Requalification/Revalidation Engineer, you’ll play a key role in the ongoing remediation program, supporting the requalification of critical equipment—including autoclaves, washers, and controlled temperature units (CTUs, such as refrigerators and freezers). You’ll also be involved in the qualification and validation of biologics process equipment, offering flexibility to support both requalification and potential revalidation activities as project needs evolve.

What we’re looking for:

• Solid experience with equipment requalification and/or revalidation, especially for autoclaves, washers, CTUs (refrigerators/freezers)
• Direct experience with qualification and validation in biologics manufacturing is a strong plus
• Good understanding of GMP and regulatory requirements
• Strong documentation and technical writing skills
• Ability to adapt to changing project scopes and priorities

Join a dynamic remediation programme at one of the world’s leading pharmaceutical companies, and contribute to quality improvement in a state-of-the-art biologics manufacturing environment.