Responsibilities
- Be responsible for updating, reviewing, and archiving relevant documents within the department.
- Draft and update project batch records.
- Handle various departmental operations, including reimbursement, attendance, procurement, finance, and meeting arrangements.
- Oversee GMP training for department staff and related tasks.
- Manage Lean Management and WBS projects within the department.
- Address EHS-related tasks.
- Oversee production master planning and scheduling.
- Perform other tasks 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.
- 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.
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