Documentation & Validation Engineer
Are you ready for the next step in your career? As a technical specialist in the Life Science sector, you work on technologies that improve lives. You play a key role in the development and optimization of systems for drug production, medical devices and biotechnology, for example.
Your work is crucial to the success of these projects.
Responsibilities
* As Documentation and Validation engineer, you are responsible for the validation of automated control systems according to GMP guidelines.
* You write commissioning and qualification test protocols based on user requirements and functional specifications.
* You execute tests accurately and in compliance with GMP regulations.
* You perform risk assessments and document the outcomes clearly.
* You are the point of contact for internal and external stakeholders regarding validation topics.
* You work closely in a project team, following up on schedules and milestones.
* You have an affinity for machines and automation and an interest in accompanying documentation and testing.
Requirements
* A Bachelor's or Master's degree in a relevant technical field.
* At least 2 years of relevant experience within a GMP environment.
* Experience with GAMP5, 21CFR part 11 and CSV.
* Affinity with computerized systems, such as PLC and SCADA.
* Good analytical & communication skills.
* Willingness to travel sporadically.
* Fluent in English and good knowledge of French and/or Dutch.
At STAR, your career is our focus. We connect you with challenging projects, offer personal guidance and create opportunities with clients you are excited about.
Together we make sure you get the most out of your career.
Get in touch with our Consultant Roosmarijn
Email
r.vandewater@star-specialists.com
Phone
+32 473501831
WhatsApp
+32 473501831