Pharmaceutical MES Integration Specialist

2 weeks ago

Ellore, Andhra Pradesh, India beBeeRegulatory Full time ₹ 15,00,000 - ₹ 25,00,000
Job Description

As a seasoned MES Testing Consultant, you will play a pivotal role in ensuring the seamless integration and validation of Manufacturing Execution Systems (MES) within pharmaceutical manufacturing environments. Your expertise will be crucial in supporting and validating MES platforms, driving regulatory compliance, and fostering a culture of excellence.

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 to ensure accuracy and compliance.
  • Conduct rigorous regression, functional, and integration testing to guarantee system stability and performance.
  • Support User Acceptance Testing (UAT), log test results, and manage deviations in accordance with industry standards.
  • Document test evidence and participate in internal and external audits to maintain regulatory compliance.
Requirements:
  • Minimum 5 years of experience in MES Testing with a strong understanding of GMP guidelines and FDA regulatory compliance.
  • Hands-on experience with MES platforms such as Werum PAS-X, Rockwell PharmaSuite, or similar is essential.
  • Solid communication, documentation, and analytical skills are required to effectively collaborate with cross-functional teams.
  • Experience in pharmaceutical or life sciences environments is preferred but not necessary.
Benefits:

As an esteemed MES Testing Consultant, you will enjoy the benefits of working with a reputable organization, including a competitive compensation package, opportunities for growth and professional development, and a collaborative work environment.

Others:

The ideal candidate will possess excellent problem-solving skills, be detail-oriented, and have a passion for delivering high-quality results in a fast-paced environment.

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