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