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Senior Process Engineer Validation
2 weeks ago
This project involves managing and implementing Sterilizing In Place (SIP) systems within the pharmaceutical industry. The role requires expertise in clean steam sterilization processes and equipment, with a willingness to work hands-on conducting tests and validation activities.
- Oversee the integration and validation of clean steam equipment in compliance with cGMP requirements.
- Collaborate with cross-functional teams to ensure successful project outcomes.
The ideal candidate has a strong technical background, practical experience in validation, and the ability to manage projects independently.