Overview:
Ability to independently complete the registration of the responsible product line to ensure registration accuracy, timeliness and completeness.
Direct, organize and coordinate RA activities for China sales organization to ensure business is conducted in compliance with regulatory, quality, safety, health and environmental requirements.
Develop and improve RA standards and procedures to achieve organizational efficiencies and ensure optimal value to Business plan.
Responsibilities:
1. Product registration
2. Operational efficiency
3. Registration process quality assurance
Qualifications:
Biologist / Pharmacist combined with relevant experiences within Diagnostic / Biological Production .
At least minimum of 3 years in a multinational organization and 2-3 years working experience on RA position.
Good learning ability and have an innovative spirit.
Good communication with CFDA and internal partner.
Good teamwork.
职能类别: 药品注册
联系方式
上班地址:酒仙桥路10号 恒通商务园
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