Associate

Roles and Responsibilities :

• Ensure compliance with Good Manufacturing Practices (GMP) guidelines during equipment handling and production processes.
• Conduct regular inspections of manufacturing areas to identify potential issues and implement corrective actions.
• Collaborate with cross-functional teams to resolve equipment-related problems and optimize production efficiency.
• Develop and maintain documentation related to equipment maintenance, calibration, and validation.

Job Requirements :

• 3-6 years of experience in pharmaceutical or life sciences industry as an Associate Production Engineer or similar role.
• Strong understanding of BMR (Batch Manufacturing Record) requirements for equipment handling and production engineering.
• Proficiency in GMP regulations and ability to apply them effectively in daily work.
• Experience with equipment handling, installation, testing, calibration, validation, cleaning validation protocols.