Job Description:

• Act as Head of Engineering in organizing and monitoring overall activities and coordination in Engineering Department.
• Carry out all engineering activities in compliance to GMP for production equipment, utility systems and facility maintenance.
• Take part in new GMP site setup, utilities and equipment installation, commissioning, qualification and routine check-up.
• Ensure the premise and all equipment running are in good condition and do not present any risk including physical, chemical and microbial, which will affect the quality of final product.
• Approve SOPs relating to engineering operation to ensure their strict implementation.
• Participate in change control, deviation, CAPA, QRM, supplier evaluation, validation, and other quality-related activities.
• Other duties as assigned by management.

Qualification and requirements:

• Bachelor's Degree in Mechanical Engineering, Electronic/Electrical Engineering, Building Service Engineering or related disciplines or above; and
• At least 3 years of relevant experience in GMP pharmaceutical manufacturing (at managerial or supervisory level) in one or more pharmaceutical manufacturers.
• Excellent communication, problem-solving, time management and prioritization skills.
• Self-motivated and willing to accept temporary responsibilities outside of initial job description.

To apply, please email your CV and covering letter explaining why you want to work for Novoheart.