Associate Manufacturing Support Engineer

Responsibilities

• Be responsible for the preparation of buffers and media for drug substance manufacturing according to GMP.
  
  
• Participate in and execute production projects, completing production plans on time.
  
  
• Complete production records in accordance with GMP requirements.
  
  
• Assist in drafting/ upgrading SOPs, URS, PQ, and other documents.
  
  
• Perform other tasks as assigned by leadership.
  
  

Requirements

• Diploma or higher qualification in Biological, Chemical, Pharmaceutical Engineering, or other related specialties; candidates with equivalent work experience will also be considered.
  
  
• Ability to adapt to a GMP cleanroom environment, including the requirement to wear dust-free clothing, masks, and goggles.
  
  
• Possess good communication and comprehension ability.
  
  
• Display good working attitude, strong work ethic, and team collaboration
• Be open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.
  
  

Career Development

• Comprehensive in-house training program (E-learning / OJT / Mentorship)
• Dual career development tracks – Professional & Managerial Tracks
• Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment
• Cross cultural learning
• GMP greenfield start-up experience