太仓招聘

Position Responsibilities
1. Responsible for securing the registration of local products and imported products.
2. Responsible for implementing regulatory requirements into planning for developing products and changed products.
3. Mornitor SFDA regulatory changes and drive awareness and implementation of changed regulatory requirements.
4. Responsible for type testing
5. Assist clinical trial when necessary.

Experience Required
1. At least two years of IVD product registration experience.
2. Clinical trial experience of IVD product is highly perfered.
3. Good knowledge of medical device/IVD development processes, clinical trial monitoring procedures, medical terminology.
4. Excellent organizational, teamwork and problem solving skills and communication skills.
5. Good computer skills
6. Fluent English skill in writing and reading. Fluently spoken English preferred.

PerkinElmer Instruments (Shanghai) Co.,Ltd ( US company)

PerkinElmer is a global scientific leader providing an extensive range of technology solutions and services to address the most critical issues facing humanity. From critical research and prenatal screening to environmental testing and industrial monitoring, we’re actively engaged in improving health and enhancing quality of life all around the world.
PerkinElmer’s proud history dates back to the 1930s.Our legacy of scientific advancement, operational excellence and continual expansion, from Boston to Beijing, is the foundation of our mission to improve human and environmental health.
Collaborating with customers to identify risks, discover and monitor the things that matter most—from safer drinking water to cleaner air, faster research to healthier babies—is imperative to executing our mission.
Encouraging ingenuity and exploration; integrity and generosity; and, teamwork and employee development is essential to living our mission, every day.