職務要求

• Assist CSO with daily planning and testing schedule.

• Support utility system validation.

• Manage the microbiology testing and environmental monitor in the pilot lab.

• Participate in tech transfer from cooperating partners.

• Collaborate with other departments to set up the GMP system in the new facility.

• Provide the guide to junior people.

• Review and draft the related SOPs.

任職資格

• Master's Degree in biology, microbiology, or other related majors.

• Above 5 years of working experience in the cGMP Biotech/Pharmaceutical industry area is necessary.

• Experience in environmental monitor and microbiology testing is necessary.

• Familiar with USP, EP, WHO, ICH, and PIC/S GMP guidance.

• Good verbal and English writing skills are needed.

• Writing skills, organization skills, and communication skills to cooperate with the team and other departments.

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