CSV Engineer (Pharma)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
CSV Engineer (Pharma): Support validation and qualification activities for computerized systems in a pharmaceutical environment with an accent on compliance with GxP regulations and internal protocols. Focus on preparing and reviewing validation documentation, training end users, and collaborating on system integration and improvements.
Hybrid • Boxmeer (Netherlands)
Company
IT consultancy firm that helps startups, mid-sized and large corporations create and deliver innovative technologies including AI, ML, BI, Web, and Automation for industries like Pharma.
What you will do
- Prepare, review, and approve validation documentation.
- Maintain accurate and compliant validation records.
- Support validation and qualification activities for computerized systems.
- Ensure systems are used in line with GxP regulations and internal protocols.
- Train end users on proper system usage and compliance requirements.
- Collaborate with cross-functional teams to support system integration and improvements.
Requirements
- Bachelor's degree in IT, Business, or related field (or equivalent experience).
- Experience working in a GxP-regulated environment.
- Understanding of computerized system validation (CSV) processes.
- Ability to work independently with moderate supervision.
- Strong adaptability and problem-solving mindset.
- Excellent written communication skills in English.
Nice to have
- Knowledge of automation systems (ISA-95 level 2/3).
- Experience with SDLC (Systems Development Lifecycle).
- Exposure to manufacturing systems or pharma environments.
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