Associate Process Engineer - Night Shift

Role: Associate Process Engineer supporting manufacturing improvements, validation, and automation in a pharmaceutical plant. Responsibilities: assist in process optimization to enhance yield, quality, and equipment reliability; develop and update SOPs; conduct process validation, simulations, and equipment qualification; troubleshoot manufacturing issues; analyze data to drive process enhancements; review protocols and reports; support CAPA activities and deviations; collaborate with vendors and cross-functional teams to ensure compliance with cGMP and FDA regulations. Requirements: Bachelor's degree in Engineering, Pharmaceutics, or related field; 0-3 years in pharmaceutical manufacturing or engineering; strong problem-solving, data analysis, and technical documentation skills. Preferred: Master's degree in relevant fields. High-Value: pharmaceutical manufacturing, process validation, cGMP, FDA compliance, data-driven process improvement, support for continuous manufacturing enhancements. WorkSetup: not specified; likely on-site based on manufacturing environment.