Deputy Manager, Manufacturing

Job Description

This role is responsible for managing and overseeing pharmaceutical manufacturing operations at a deputy manager level within a regulated manufacturing environment, ensuring that all production activities are conducted in compliance with current Good Manufacturing Practices, production schedules, and applicable regulatory requirements. The position provides senior oversight and leadership to manufacturing personnel, ensuring operational quality and compliance standards are consistently met across all manufacturing activities. It ensures that all manufacturing operations are conducted in strict adherence to validated procedures, cGMP standards, and regulatory requirements. The role collaborates with quality, engineering, and production planning teams to optimize manufacturing processes, resolve technical issues, and implement process improvements. It monitors manufacturing process parameters and equipment performance, identifying and addressing deviations as required. The position develops and implements process improvement initiatives to enhance manufacturing quality, cost efficiency, and production scheduling. It operates within a highly regulated pharmaceutical environment, ensuring all manufacturing outputs meet defined quality and compliance standards. The role also supports training and development of manufacturing team members to build operational capability.

• Manage and oversee pharmaceutical manufacturing operations at a senior level, ensuring all activities comply with validated procedures, cGMP standards, and regulatory requirements

• Provide senior oversight and leadership to manufacturing personnel, ensuring operational quality and compliance standards are consistently met

• Monitor manufacturing process parameters and equipment performance, identifying and addressing deviations as required

• Collaborate with quality, engineering, and production planning teams to optimize manufacturing processes and resolve technical issues

• Ensure accurate and complete batch documentation records including batch manufacturing records and equipment usage logs are maintained

• Develop and implement process improvement initiatives to enhance manufacturing quality, cost efficiency, and production scheduling

• Ensure all manufacturing activities comply with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements including FDA and EMA guidelines

• Support training and development of manufacturing team members to build operational capability

• Participate in cross-functional projects and initiatives to enhance manufacturing quality and operational efficiency

• B. Pharm B. Pharm - Required

• M. Pharm M. Pharm - Preferred

• 8 years or more in 8 - 10 Years

Categories