Intro:

In this function, you play a key role in delivering high-quality technical documentation for innovative engineering projects. You will create manuals, validation and commissioning documents, and support quality-driven processes in a dynamic pharmaceutical and industrial environment. This is an excellent opportunity for a detail-oriented professional who combines technical expertise with a passion for accuracy and compliance.

Function-information:

- To write the technical documentation e.g. manuals, work instructions, parts list, …
- To compose documents for e.g. commissioning, IQ, OQ, risk analysis, CSV, …
- To follow up the documentation and validation related matters in our production as well as at the customer site.

Function-requirement:

- Technical bachelor's degree (or higher) or equivalent by experience.
- Customer focus with an accurate and analytical approach.
- You place high value on quality.
- You are fluent in English and Dutch
- At least 2 years relevant experience
- Knowledge in the pharmaceutical industry and especially in GMP/GAMP is an asset.
- Knowledge of office applications: Word, Excel, Outlook

📌 Documentation engineer (España)
🏢 Netwerk
📍 España