
Associate Manufacturing Support Engineer
2 days ago
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
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