8 дней назад
GS APAC Regulatory Information Administrator-1 (MedTech)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
GS APAC Regulatory Information Administrator-1 (MedTech) (MDRiM/regulatory data): Managing regulatory information and data quality for APAC MedTech regulatory activities with an accent on license maintenance, data analysis, and database integrity. Focus on coordinating regulatory data across APAC markets, maintaining MDRiM trackers and strategies, and improving regulatory processes.
Location: Taguig, National Capital Region (Manila), Philippines. Working hours: 8am SGT – 5pm SGT.
Company
Johnson & Johnson MedTech develops surgical, orthopedic, interventional, and other healthcare solutions as part of Johnson & Johnson’s global healthcare organization.
What you will do
- Monitor and complete regulatory impact assessments in the MDRiM system, including maintaining license information.
- Extract required information from data sources and perform analyses for APAC Regulatory Affairs requests.
- Create and maintain trackers and databases to ensure data accuracy and integrity.
- Coordinate with APAC markets to maintain accurate regulatory data representation.
- Maintain local and regional regulatory strategies and actions in MDRiM.
- Support process improvement, regulatory forecasting, and execution planning activities.
Requirements
- Bachelor’s degree required; Business, Finance, Sales, or Marketing concentration preferred.
- 3+ years of professional experience, preferably in medical devices, surgery, healthcare, or medical data administration.
- Proficiency in English and effective communication skills for interacting with local Regulatory Affairs users.
- Strong skills in CSV, Excel, Power BI, and relational database management systems.
- Ability to follow detailed procedures, escalate issues appropriately, and execute plans accurately.
- Strong attention to detail, compliance, data integrity, discipline, and cross-functional collaboration.
Nice to have
- Experience in Regulatory, Quality, or Clinical functions within medical device or pharmaceutical organizations.
- Experience in a shared services center of a multinational corporation.
Culture & Benefits
- Work within a global services network spanning professionals in more than 60 countries.
- Participate in innovation and business process improvement initiatives.
- Collaborate with APAC MedTech Regulatory Affairs teams and stakeholders across markets.
- Inclusive and equal-opportunity work environment.
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