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À propos
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.
Contract: Full-time Freelance / Contract
Duration: Long-term project phase
Start: Immediate
Project Type: Pharmaceutical Automation & Validation
We are supporting a large pharmaceutical facility in the search for experienced CSV Engineers with strong SCADA and PCS7 expertise. The project is entering system qualification and integration phase and requires professionals with proven validation experience in regulated GMP environments.
Key Responsibilities
- Execute CSV documentation and protocol testing
- Validate SCADA and Siemens PCS7 systems
- Support system integration and qualification
- Update RTMs and validation documentation
- Participate in FAT/SAT activities
- Collaborate with automation and CQV teams
- Ensure data integrity and compliance standards
Requirements
- Strong CSV experience in pharma
- Hands‑on SCADA validation background
- Experience with Siemens PCS7 (essential)
- Knowledge of GMP and data integrity requirements
- Ability to execute protocols independently
- On‑site availability required
If this opportunity aligns with your background, please send your CV to and I will contact you to discuss next steps.
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Compétences linguistiques
- English
Avis aux utilisateurs
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