Esenar Pharma Enterprises

2 Job openings at Esenar Pharma Enterprises
Senior Validation Engineer Telangana,India 0 years Not disclosed On-site Full Time

Role Description This is a full-time, on-site role for a Senior Validation Engineer located in Telangana, India. The Senior Validation Engineer will be responsible for developing and executing validation protocols for pharmaceutical manufacturing. Daily tasks will include ensuring compliance with Good Manufacturing Practices (GMP), coordinating with cross-functional teams, conducting process validation, equipment validation, and cleaning validation. The role also involves troubleshooting and debugging validation issues to maintain production efficiency and quality. Qualifications Experience in Good Manufacturing Practice (GMP) and Validation Proficiency in RTL Design and Functional Verification Strong debugging skills Bachelor's degree in Engineering, Science, or a related field Excellent analytical and problem-solving skills Effective communication and teamwork abilities Prior experience in the pharmaceutical industry is a plus Show more Show less

Senior Validation Engineer telangana 5 - 9 years INR Not disclosed On-site Full Time

Role Overview: You will be a Senior Validation Engineer based in Telangana, India, responsible for developing and executing validation protocols for pharmaceutical manufacturing. Your daily tasks will involve ensuring compliance with Good Manufacturing Practices (GMP), coordinating with cross-functional teams, conducting process validation, equipment validation, and cleaning validation. Additionally, you will be troubleshooting and debugging validation issues to uphold production efficiency and quality. Key Responsibilities: - Develop and execute validation protocols for pharmaceutical manufacturing - Ensure compliance with Good Manufacturing Practices (GMP) - Coordinate with cross-functional teams for validation processes - Conduct process validation, equipment validation, and cleaning validation - Troubleshoot and debug validation issues to maintain production efficiency and quality Qualifications Required: - Experience in Good Manufacturing Practice (GMP) and Validation - Proficiency in RTL Design and Functional Verification - Strong debugging skills - Bachelor's degree in Engineering, Science, or a related field - Excellent analytical and problem-solving skills - Effective communication and teamwork abilities - Prior experience in the pharmaceutical industry is a plus,