Engineer, Validation Engineer

Job Title
CQV Engineer

Sector
Pharmaceutical / Medical Device Manufacturing

Role
The CQV Engineer is responsible for commissioning, qualification, and validation activities within a GMP manufacturing environment. The role focuses on hands‑on execution and documentation for secondary packaging systems, ensuring systems meet regulatory and internal requirements. The position reports to Validation & Compliance within Site Engineering.

Non‑Negotiable Requirements

Degree in Engineering or related technical discipline

Minimum 3 years of CQV experience in a pharmaceutical or medical device manufacturing environment

Hands‑on commissioning and qualification experience in secondary packaging operations

Experience with secondary packaging equipment using print and inspection systems

Computerized Systems Validation (CSV) experience

Experience creating GMP‑compliant CQV documentation

Experience developing validation and commissioning plans

Experience performing risk assessments and criticality assessments

Experience executing IQ, OQ, and PQ activities

Experience writing test protocols and validation reports

Experience creating requirement traceability matrices

Experience supporting engineering projects in a GMP environment

Experience with Systech systems

Experience with Cognex vision systems

Experience working independently or with remote teams

Experience supporting multiple project phases from design through validation

Practical Information

Location:

Breda, The Netherlands

Start Date:

ASAP

Work Model:
Full time

Send your CV or inquiries to:  

Seniority level
Mid‑Senior level

Employment type

Full‑time

Job function
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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