EMPREGO MEDICAL DEVICE REGULATORY SPECIALIST

Provides consultation on regulatory requirements related to medical device submissions for assigned divisions and in support of corporate initiatives...

Performs work alongside medical safety colleagues and under supervision of the medical director/ medical safety manager... ⦁    applies working knowledge of medical...

Quality systems, r&d, quality, post market) within the medical device, ivd, pharmaceutical or healthcare industries working knowledge of fda, eu and/or international...

Additionally, the specialist is responsible for assessment of device changes for regulatory implications...     about this role:  the senior regulatory specialist...

This role will be responsible for regulatory affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing...

Your responsibilities will include:  support sterilization process owner and global regulatory processes, responsibilities include the following: support regulatory...

About this role:  with adequate supervision, the regulatory affairs specialist iii is responsible for planning, managing, and implementing regulatory submissions...

We cover all therapy areas including medical device...   job description the specialist, regulatory and pv network is responsible for providing the strategy based...

Manages meetings with regulatory agencies... may write new regulatory standard operating procedures, and propose revisions or act as reviewer for regulatory standard...

Other duties include back-up support of senior regulatory manager  mainly regulatory support for r&d, marketing, pva, legal... this person is also responsible...

Participate in activities to ensure compliance with worldwide regulatory requirements...   you will have the opportunity to discuss your preferred working location...

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population...

• inform team members of completion of regulatory contractual... we create intelligent connections to accelerate the development and commercialization of innovative...

Therapeutic area expertise: leverage your medical expertise throughout the device life cycle and serve as a medical advisor for regulatory matters...

), preferably in a medical device company... high school diploma or ged or associate degree with a minimum 4 years in a clinical specialist or related medical role...

Within the glt, the launch specialist will maintain an individual and primary focus on clinical support and customer engagement...  the role will afford the launch...

Mc medical, a werfen company mc medical is a company of the werfen group... it is a pioneer in the commercialization of medical devices in portugal and is currently...

You are responsible for facilitating or executing specific regulatory writing needs of assigned therapeutic areas and/or products as well as abstracts, presentations...