
MES System Testing Specialist
4 days ago
We are seeking a skilled MES testing professional to support and validate Manufacturing Execution Systems (MES) used in pharmaceutical manufacturing environments.
- The ideal candidate will have extensive knowledge of MES platforms, 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.
- Hands-on experience with MES platforms such as Werum PAS-X 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.
As an MES system testing specialist, you will play a crucial role in ensuring the seamless operation of our Manufacturing Execution Systems. Your expertise in MES platforms, test lifecycle processes, and regulatory compliance will enable us to maintain high-quality standards in our pharmaceutical manufacturing environment.
Our company is committed to delivering high-quality products and services. As an MES system testing specialist, you will be part of a team that prioritizes quality and excellence. You will work closely with cross-functional teams to ensure that our Manufacturing Execution Systems meet the highest standards.
If you are a motivated and detail-oriented individual who is passionate about quality and excellence, we encourage you to apply for this exciting opportunity. Join our team and contribute to delivering exceptional results in the pharmaceutical manufacturing industry.
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