
Expert MES Validation Specialist
21 hours ago
We are seeking a highly skilled and experienced Manufacturing Execution Systems (MES) Testing Consultant to support the validation of MES platforms used in pharmaceutical manufacturing environments.
The ideal candidate will possess in-depth knowledge of MES testing, test lifecycle processes, and regulatory compliance in the life sciences industry.
Key Responsibilities:
- Develop and execute comprehensive test plans, test cases, and test scripts for MES implementations.
- Validate electronic batch records, logbooks, and process flows in MES platforms.
- Conduct thorough regression, functional, and integration testing.
- Support User Acceptance Testing (UAT), log test results, and manage deviations.
- Document test evidence and participate in internal and external audits.
Requirements:
- Minimum 5 years of experience in MES testing with hands-on experience with MES platforms such as Werum PAS-X, Rockwell PharmaSuite, or similar.
- Solid understanding of GMP guidelines and FDA regulatory compliance.
- Experience in pharmaceutical or life sciences environments is preferred.
- Strong communication, documentation, and analytical skills are required.
This role offers the opportunity to work with leading-edge technology and contribute to the development of high-quality MES systems that drive innovation in the pharmaceutical industry.
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