GMP Validation Consultant — Onsite Projects & Growth

Trevalco BV; Town of Belgium (WI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

CAO90 bonus

Hospitalisation and dental care insurance

Meal vouchers

Company car or mobility budget

Job summary

Trevalco BV is seeking a Validation Consultant to work with clients in the pharmaceutical industry across various validation projects. Responsibilities include developing validation strategies, writing validation plans, and managing quality records. Candidates should be fluent in English and Dutch, possess strong analytical and communication skills, and hold a Master’s degree in science or engineering.

Enjoy a competitive salary, training opportunities, and a healthy work/life balance. Join a Belgian SME and make an impact!

Qualifications

• Strong analytical skills, well organized, studious and precise.
• Enjoy managing documentation: creating, reviewing, and updating.
• Ability to explain, convince, and correct with excellent communication.

Responsibilities

• Develop a validation strategy that meets regulatory and client expectations.
• Write validation plans and reports.
• Manage quality records such as deviations and CAPAs.
• Advise on pharmaceutical regulatory requirements.

Skills

Fluent in English

Fluent in Dutch

Strong analytical skills

Perfect communication skills

Education

Master degree in science or engineering

Job description

Trevalco BV is seeking a Validation Consultant to work with clients in the pharmaceutical industry across various validation projects. Responsibilities include developing validation strategies, writing validation plans, and managing quality records. Candidates should be fluent in English and Dutch, possess strong analytical and communication skills, and hold a Master’s degree in science or engineering.

Enjoy a competitive salary, training opportunities, and a healthy work/life balance. Join a Belgian SME and make an impact!