TRABAJO REGULATORY AFFAIRS MEDICAL DEVICES

We propose and support medical education programs that meet unmet medical needs (clinical questions)... • practice fair and neutral medical and scientific communication...

To act as the medical affairs expert and drive a unified emea medical voice... to drive the implementation of the activities outlined in the emea medical affairs...

Close collaboration with the regional medical affairs representatives to develop integrated global medical affairs strategies and plans and maintain open, two-way...

The position reports to the regional regulatory affairs manager, emea... write regulatory assessments for pirs and regulatory points of view (pov) as needed...

The cardiovascular & specialty solutions (css) group, part of the medical tech sector within johnson & johnson, is recruiting for a manager, regulatory affairs...

• preparation of regulatory documentation of medical devices (including ivds and medical device software)...  your main responsibilities: reporting to the medical...

Associate regulatory affairs strategist   the associate regulatory affairs strategist plays a role in providing consultation to veristat’s clients, in translating...

Awareness or regulatory affairs environment, eu-wide legal framework, and european authorities’ websites... profilewe are looking for a dynamic, capable, curious...

Essential skills/experience: bachelor's degree in science, regulatory sciences or pharmacy experience in regulatory / drug development (industry or health authority)...

Johnson & johnson medtech india is recruiting for a medical affairs lead located in mumbai, india...   position overview: lead medical affairs for one ethicon...

·       represents regulatory affairs on cross-functional project teams... ·       a scientific and technical understanding of medical...

Job description: we seek a regulatory affairs manager to lead our roadmap in ce-ivdr...   •team leadership •s elf-taught person   candidate requirements: • advanced...

The role: the senior regulatory affairs associate has responsibility for providing comprehensive regulatory services to clients within the pharmaceutical, biologic...

Previous experience in medical devices is mandatory... together, our dedicated, diverse global team is shaping an exciting future for zimvie— we hope you’ll consider...

Provide quality oversight during risk assessments, part 11, annex 11, and regulatory evaluations... we are looking for a " quality assurance consultant (software...

Knowledge of medical devices related to the treatment of heart disease knowledge of clinical operations such as clinical trials according to gcp and pms according...

As a clinical research associate (cra) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines...

Product safety and regulatory requirements •                    ...