Reviewer (m/f/d) Validation Documents

SMP GmbH is a DIN EN ISO/IEC 17025-accredited testing laboratory offering a wide range of services related to cleaning, disinfection, and sterilization processes. We support manufacturers of medical devices by helping them introduce new products and by regularly testing products and devices in hospitals and medical practices.

To strengthen our validation team, we are looking for motivated and qualified individuals to join us as reviewers (m/f/d) of validation documents in the ProVal department.

Your responsibilities

As a reviewer in the ProVal department, you will play a key role in ensuring the quality of our validation processes. Your main tasks will include:

• Technical, factual, and normative review of validation documents in accordance with current review criteria and within defined deadlines.
• Communicating with internal and external validators to coordinate necessary corrections to reports.
• Documenting and archiving the reviewed documents in the electronic document system.
• Issuing print approvals to external service providers.
• Responsible role with direct influence on invoicing and project progress.

Your profile

• Technical or scientific education.
• Desirable: Experience in validation or in working with RDGs, sealing devices, or sterilizers.
• A careful and structured approach to work.
• Confident use of digital document systems.
• Strong communication skills and the ability to work in a team.
• Ability to work independently and plan your own schedule.

What we offer

• Flexible working hours: You can plan and scale the work freely in terms of time.
• Remote work: Work completely from home.
• Structured training by experienced mentors.

Interested? Send your application to bewerbung@smpgmbh.com.