【飞利浦中国招聘信息】诚聘【Sr. Regulatory Affairs Specialist】年薪30-45k,飞利浦中国公司规模10000人以上,经验:5-10年,学历: 统招本科,猎聘祝您顺利获得飞利浦中国Sr. Regulatory Affairs Specialist职位.
?Bachelor’s degree or above, major in medical science, biomedical engineering or related field, safety engineering background will be preferred ?5+ years’ experience in medical device regulatory affairs, previous experience in drafting CER and submission with clinical trial data is a plus ...
Goals/Mission To assist Chief RepresentativeANDadminister regulatory affairs by coordinating with the Chinese authority and external partners onMedical Deviceregistration. To monitor the regulation updates and new registration cases in industry that LM Group involved. To prepare the annual cost budget for ...
Regulatory Affairs Specialist | Process Improvement | IVD Knowledge +1-(234)-555-1234 help@enhancv.com linkedin.com San Diego, California Summary With over 7 years of regulatory experience in the medical device industry, my expertise spans across compliant market entry, efficient process management,...
UK Responsible Person Miriam, Head of Quality Management and Regulatory Affairs I have worked, and I am still working, with OMC Medical for our medical device project. We have worked with OMC Medical to write technical documentation for our product which includes CE marking, FDA marking and UK...
The Regulatory Affairs Specialist is responsible for providing regulatory CMC support through the product life cycle. These job responsibilities include but are not limited to regulatory strategies, submission timeline development, change control, and preparing submission documents. ...
The FDA is ALWAYS Watching Think that the FDA won’t notice your “therapeutic massager” device? Think they have much bigger fish to fry than your Learn More EU MDR Part 1: Logical Evolution or Legislative Overreach? First in a series of blogs based on a conversation about EU MDR with ...
Giulia Girola, Regulatory Affairs Specialist, Materialise Leon Doorn, Chair, NEN Stuart Angell, Managing Director, IVDeology Ltd Vaso Basinou, Clinical Evaluator and Project Manager (Clinical/Medical/Regulatory Affairs) Cli...
AREMA is specialized in Regulatory Affairs, for Pharmaceutical, medical devices and Health Care industries and offers also other services, marketing and commercial opportunities in many countries. AREMA have multiple services such as: Strategic and reg
Regulatory Affairs / Medical / EU / Risk Managment Domain: HealthCare, Pharmaceuticals DBSI Services Bridgewater, NJ Post Resume to View Contact Details & Apply for Job Job Description: Job Title: Regulatory Affairs Specialist Location: US-CA-Northridge ...