Job Duty:
- Maintain production environment and quality system to reach ISO 13485 standard.
- Draft, update and daily recording for production documentations such as SOP, WIs, DHR and record to maintain the documentation system for production department.
- Responsible for equipment qualification, maintenance and calibration.
- Responsible for production and materials planning and controlling.
- Responsible for on-hands manufacturing work, including reagent preparation, medical device manufacturing, site cleaning and in-process checking according to WIs and SOP.
- On-job-training would be provided for all the above duty.
Requirement:
- Higher Diploma, Bachelor degree, or above in Life Sciences / Biomedical Sciences / Biotechnology / Biochemistry / Biotechnology / Biological Science / Microbiology / Bioengineering / Biomedical Engineering / Chemical Engineering / Chemistry /Chemical Technology or equivalent in science and engineering.
- Team-player and self-motivation, work in a logical systematic manner, willing to learn and with good communication and problem-solving skills.
- Experience in laboratory/ manufacturing/ production field is a plus.
- Some knowledge in regulatory such as ISO9001, ISO13485, GMP, FDA guideline is a plus.
- Experience with MS Office.
- Fresh Graduates are welcome.
We offer an attractive remuneration package including competitive salary, 5-day work, annual leave and medical insurance. If you are interested in this career opportunity, please apply with your detailed resume, present and expected salary by clicking hr@sanwabiotech.com
Personal data collected will be used for recruitment purpose only.