Sr. RA Specialist-1420043W
Description
Johnson & Johnson is the world's most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. The more than 250 Johnson & Johnson operating companies employ approximately 118,000 men and women in 60 countries and sell products throughout the world.
嬌生集團是全球最具多元性、業務分布範圍最廣的醫療保健用品公司業，我們的產品與服務每天觸及全球近十億生命。我們的足跡遍佈消費品、製藥以及醫療器材與診斷產品市場，提供解決世界主要健康議題的技術與資源。我們在全球60個國家設立250多家營運公司，員工接近12萬人，產品銷售世界各地。
Key Responsibilities
- Timely product registration, license renewal and variation of OTC brand.
- Monitor and communicate the potential/confirmed regulatory changes/new regulations with key business partners based on the robust assessment of regulatory implications and business impact.
- Effective liaison with TFDA and TPE DOH on the affected regulatory topics
- Regulatory review/approval of all the package claims and advertisements
- Support the SRC audit in Dec.
Qualifications
- 1~2 yrs registration experiences in RA of pharmaceutical industry or censorship.
- Bachelor’s degrees or above
- Knowledge in Chemistry, Pharmacy
- Good inter-personal skills
- Proactive & positive & innovative & flexible mindset
- Strong analytical, problem solving and independent project management skills with minimum coaching/guidance
- Good communication skill
- Good English communication (Writing & Verbal) ability
- MS Office skills (Word, PPT, Excel, Outlook) proficiency
Primary Location:Asia Pacific-Taiwan-Taipei-Taipei
Organization: Johnson & Johnson Taiwan, Ltd. (8580)
Job Function: Regulatory Affairs
Description
Johnson & Johnson is the world's most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. The more than 250 Johnson & Johnson operating companies employ approximately 118,000 men and women in 60 countries and sell products throughout the world.
嬌生集團是全球最具多元性、業務分布範圍最廣的醫療保健用品公司業，我們的產品與服務每天觸及全球近十億生命。我們的足跡遍佈消費品、製藥以及醫療器材與診斷產品市場，提供解決世界主要健康議題的技術與資源。我們在全球60個國家設立250多家營運公司，員工接近12萬人，產品銷售世界各地。
Key Responsibilities
- Timely product registration, license renewal and variation of OTC brand.
- Monitor and communicate the potential/confirmed regulatory changes/new regulations with key business partners based on the robust assessment of regulatory implications and business impact.
- Effective liaison with TFDA and TPE DOH on the affected regulatory topics
- Regulatory review/approval of all the package claims and advertisements
- Support the SRC audit in Dec.
Qualifications
- 1~2 yrs registration experiences in RA of pharmaceutical industry or censorship.
- Bachelor’s degrees or above
- Knowledge in Chemistry, Pharmacy
- Good inter-personal skills
- Proactive & positive & innovative & flexible mindset
- Strong analytical, problem solving and independent project management skills with minimum coaching/guidance
- Good communication skill
- Good English communication (Writing & Verbal) ability
- MS Office skills (Word, PPT, Excel, Outlook) proficiency
Primary Location:Asia Pacific-Taiwan-Taipei-Taipei
Organization: Johnson & Johnson Taiwan, Ltd. (8580)
Job Function: Regulatory Affairs