Generate ideas, conduct tests, and develop reports on product evaluations, refining processes to improve yield and cost
- Develop secondary packaging and artwork that meets Marketing and Regulatory requirements
- Foster effective communications between teams and departments to support company needs
- Investigate production deviations, perform material qualification, and support scale-up production trials
- Carry out engineering runs, process validation, and mitigate process gaps, ensuring compliance with specifications (QTPP, CQA, etc.)
- Handle change control, investigations, corrective actions, dossier writing, and ensure proper documentation for new product releases
- Master Degree in Biomedical Engineering/Chemical Engineering/Material Science/Physical Chemistry
- Experienced for 1-2 years in pharmaceutical or biopharmaceutical manufacturing is preferred
- Min. GPA 3.50 and TOEFL score 500. The other type of test that has equivalent value will be accepted
- Familiar with GLP, cGMP, and Industry Regulations
- Attach updated photo in CV