Urgent Freelance CQV Engineering Consultant (Pharmaceutical Industry)
Location: Northern Germany
Duration: Immediate Start - 12-Month Contract
Language: Must be German-speaking
Company Overview:
We are working exclusively with a leading pharmaceutical client to find a highly skilled CQV Engineering for a high-impact project in Northern Germany.
Key Responsibilities:
- Lead CQV for automation systems (DCS, PLC, SCADA).
- Develop process strategies for continuous improvement.
- Create and review validation documentation (protocols, reports, SOPs).
- Ensure GMP, FDA, and industry compliance.
- Troubleshoot issues during commissioning and qualification.
- Provide lifecycle support for automation systems.
- Conduct risk assessments and mitigation strategies.
- Provide lifecycle support for automation system
How to Apply:
If you're a great fit, 📩 let's connect! DM me or share a time to chat.
