
Senior MES Validation Specialist
5 days ago
We are seeking an experienced professional to support and validate Manufacturing Execution Systems (MES) used in pharmaceutical manufacturing environments.
- The ideal candidate will have deep knowledge of MES platforms, test lifecycle processes, and regulatory compliance in the life sciences industry.
Key Responsibilities:
- Develop and execute test plans, test cases, and test scripts for MES implementations.
- Validate electronic batch records, logbooks, and process flows in MES platforms.
- Conduct 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.
- 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 preferred.
- Strong communication, documentation, and analytical skills.
Benefits:
This role offers a challenging opportunity for professionals to expand their expertise and contribute to the success of our organization. As a member of our team, you will have access to cutting-edge technologies, collaborative working environment, and opportunities for growth and development.
About the Position:
This is a full-time position requiring 5+ years of experience in MES Testing. The successful candidate will be responsible for developing and executing test plans, conducting regression and integration testing, and supporting User Acceptance Testing (UAT). Strong communication and analytical skills are essential for this role.
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